A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701561



Internal ID15091527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83997047..84005144hg38UCSC Ensembl
Innerchr16:84030652..84038749hg19UCSC Ensembl
Innerchr16:82588153..82596250hg18UCSC Ensembl
Innerchr16:82588153..82596250hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg388098
hg198098
hg188098
hg178098
Variant TypeCNV gain
Copy Number
Allele State
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)nssv701561
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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