A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705015



Internal ID15094981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:47129963..47313869hg38UCSC Ensembl
Innerchr16:47163874..47347780hg19UCSC Ensembl
Innerchr16:45721375..45905281hg18UCSC Ensembl
Innerchr16:45721375..45905281hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38183907
hg19183907
hg18183907
hg17183907
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528423
Supporting Variants
Samples
Known GenesITFG1, NETO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705015
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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