A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613765



Internal ID6653973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76500726..76515970hg38UCSC Ensembl
chr7:76130043..76145287hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3815245
hg1915245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12848902, essv12848899, essv12848922, essv12848901, essv12848916, essv12848915, essv12848903, essv12848912, essv12848919, essv12848914, essv12848900, essv12848920, essv12848906, essv12848918, essv12848913, essv12848892, essv12848894, essv12848895, essv12848909, essv12848904, essv12848897, essv12848908, essv12848898, essv12848893, essv12848905, essv12848896, essv12848911, essv12848917, essv12848910, essv12848907, essv12848921
SamplesNA19146, HG02477, HG03963, HG02816, HG01882, HG03313, HG03057, NA12005, HG02314, HG02676, NA19834, NA19117, HG01917, HG03736, NA19351, HG02283, NA18498, HG02594, HG02343, HG02938, NA19175, HG03428, HG03157, NA19328, HG02947, HG03446, NA19138, NA19198, HG02642, HG02367, HG01198
Known GenesDTX2, UPK3B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613765
Frequency
Sample Size2504
Observed Gain31
Observed Loss0
Observed Complex0
Frequencyn/a


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