A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156359



Internal ID22086760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:86819561..86823329hg38UCSC Ensembl
Outerchr5:86815939..86825812hg38UCSC Ensembl
Innerchr5:86115378..86119146hg19UCSC Ensembl
Outerchr5:86111756..86121629hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg389874
hg199874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018923, nssv4018912, nssv4018905, nssv4018899, nssv4018915, nssv4018911, nssv4018919, nssv4018913, nssv4018927, nssv4018934, nssv4018931, nssv4018918, nssv4018907, nssv4018897, nssv4018922, nssv4018901, nssv4018908, nssv4018906, nssv4018929, nssv4018914, nssv4018920, nssv4018900, nssv4018917, nssv4018932, nssv4018916, nssv4018921, nssv4018898, nssv4018925, nssv4018928, nssv4018903, nssv4018924, nssv4018904, nssv4018902, nssv4018909, nssv4018933, nssv4018930, nssv4018926, nssv4018910
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156359
Frequency
Sample Size131
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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