A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522819



Internal ID15450112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16599990..16615762hg38UCSC Ensembl
Innerchr7:16639615..16655387hg19UCSC Ensembl
Innerchr7:16606140..16621912hg18UCSC Ensembl
Innerchr7:16412855..16428627hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3815773
hg1915773
hg1815773
hg1715773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698467
Samples
Known GenesANKMY2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522819
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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