A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675696



Internal ID15065662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:681725..748489hg38UCSC Ensembl
Innerchr16:731725..798489hg19UCSC Ensembl
Innerchr16:671726..738490hg18UCSC Ensembl
Innerchr16:671726..738490hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3866765
hg1966765
hg1866765
hg1766765
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516590
Supporting Variants
Samples
Known GenesCCDC78, FAM173A, FBXL16, HAGHL, JMJD8, METRN, NARFL, STUB1, WDR24
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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