A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521653



Internal ID15102260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:16275469..16292529hg38UCSC Ensembl
Innerchr6:16275700..16292760hg19UCSC Ensembl
Innerchr6:16383679..16400739hg18UCSC Ensembl
Innerchr6:16383679..16400739hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3817061
hg1917061
hg1817061
hg1717061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698271
Samples
Known GenesGMPR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521653
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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