A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700398



Internal ID15090364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81325862..81332369hg38UCSC Ensembl
Innerchr16:81359467..81365974hg19UCSC Ensembl
Innerchr16:79916968..79923475hg18UCSC Ensembl
Innerchr16:79916968..79923475hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg386508
hg196508
hg186508
hg176508
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524464
Supporting Variants
Samples
Known GenesGAN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700398
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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