A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674893



Internal ID15064859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70755935..70756382hg38UCSC Ensembl
Innerchr10:72515691..72516138hg19UCSC Ensembl
Innerchr10:72185697..72186144hg18UCSC Ensembl
Innerchr10:72185697..72186144hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38448
hg19448
hg18448
hg17448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517130
Supporting Variants
Samples
Known GenesADAMTS14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674893
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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