A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526577



Internal ID15107184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:41037763..41061603hg38UCSC Ensembl
Innerchr6:41005502..41029342hg19UCSC Ensembl
Innerchr6:41113480..41137320hg18UCSC Ensembl
Innerchr6:41113480..41137320hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3823841
hg1923841
hg1823841
hg1723841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702895
Samples
Known GenesAPOBEC2, TSPO2, UNC5CL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526577
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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