A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154699



Internal ID22085204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:209908268..209910639hg38UCSC Ensembl
Outerchr1:209897717..209913207hg38UCSC Ensembl
Innerchr1:210081613..210083984hg19UCSC Ensembl
Outerchr1:210071062..210086552hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3815491
hg1915491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007942, nssv4007891, nssv4007925, nssv4007862, nssv4007931, nssv4007865, nssv4007896, nssv4007869, nssv4007908, nssv4007930, nssv4007893, nssv4007880, nssv4007885, nssv4007894, nssv4007929, nssv4007863, nssv4007947, nssv4007864, nssv4007868, nssv4007887, nssv4007897, nssv4007940, nssv4007926, nssv4007874, nssv4007905, nssv4007901, nssv4007907, nssv4007935, nssv4007921, nssv4007920, nssv4007876, nssv4007946, nssv4007904, nssv4007875, nssv4007914, nssv4007911, nssv4007919, nssv4007937, nssv4007936, nssv4007943, nssv4007884, nssv4007941, nssv4007924, nssv4007928, nssv4007881, nssv4007912, nssv4007917, nssv4007916, nssv4007913, nssv4007886, nssv4007927, nssv4007910, nssv4007890, nssv4007888, nssv4007922, nssv4007923, nssv4007892, nssv4007873, nssv4007877, nssv4007882, nssv4007918, nssv4007899, nssv4007871, nssv4007883, nssv4007900, nssv4007872, nssv4007909, nssv4007866, nssv4007906, nssv4007879, nssv4007944, nssv4007945, nssv4007889, nssv4007878, nssv4007867, nssv4007933, nssv4007934, nssv4007895, nssv4007870, nssv4007903, nssv4007915, nssv4007902, nssv4007939, nssv4007938, nssv4007898, nssv4007932
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154699
Frequency
Sample Size131
Observed Gain0
Observed Loss86
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer