A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517727



Internal ID15098334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84397175..84397270hg38UCSC Ensembl
Innerchr16:84430781..84430876hg19UCSC Ensembl
Innerchr16:82988282..82988377hg18UCSC Ensembl
Innerchr16:82988282..82988377hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3896
hg1996
hg1896
hg1796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653023, nssv687444, nssv673785, nssv691377, nssv658188
Samples
Known GenesATP2C2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517727
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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