A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700267



Internal ID15090233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83996684..83997047hg38UCSC Ensembl
Innerchr16:84030289..84030652hg19UCSC Ensembl
Innerchr16:82587790..82588153hg18UCSC Ensembl
Innerchr16:82587790..82588153hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38364
hg19364
hg18364
hg17364
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517566
Supporting Variants
Samples
Known GenesNECAB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700267
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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