A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522898



Internal ID15103505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8685733..8769133hg38UCSC Ensembl
Innerchr16:8779590..8862990hg19UCSC Ensembl
Innerchr16:8687091..8770491hg18UCSC Ensembl
Innerchr16:8687091..8770491hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3883401
hg1983401
hg1883401
hg1783401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698556
Samples
Known GenesABAT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522898
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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