A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698262



Internal ID15434914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:43864440..43866514hg38UCSC Ensembl
Innerchr6:43832177..43834251hg19UCSC Ensembl
Innerchr6:43940155..43942229hg18UCSC Ensembl
Innerchr6:43940155..43942229hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382075
hg192075
hg182075
hg172075
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521642
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698262
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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