A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659499



Internal ID15049465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70690022..70737376hg38UCSC Ensembl
Innerchr16:70723925..70771279hg19UCSC Ensembl
Innerchr16:69281426..69328780hg18UCSC Ensembl
Innerchr16:69281426..69328780hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3847355
hg1947355
hg1847355
hg1747355
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517391
Supporting Variants
Samples
Known GenesVAC14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659499
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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