A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664730



Internal ID15401382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1261332..1299928hg38UCSC Ensembl
Innerchr16:1311333..1349929hg19UCSC Ensembl
Innerchr16:1251334..1289930hg18UCSC Ensembl
Innerchr16:1251334..1289930hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3838597
hg1938597
hg1838597
hg1738597
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515770
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664730
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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