A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520122



Internal ID15100729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80921496..80968018hg38UCSC Ensembl
Innerchr16:80955393..81001915hg19UCSC Ensembl
Innerchr16:79512894..79559416hg18UCSC Ensembl
Innerchr16:79512894..79559416hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3846523
hg1946523
hg1846523
hg1746523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672073, nssv676419, nssv682802, nssv683209, nssv660974, nssv682675
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520122
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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