A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524978



Internal ID15105585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21211275..21217954hg38UCSC Ensembl
Innerchr16:21222596..21229275hg19UCSC Ensembl
Innerchr16:21130097..21136776hg18UCSC Ensembl
Innerchr16:21130097..21136776hg17UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg386680
hg196680
hg186680
hg176680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701007
Samples
Known GenesZP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524978
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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