A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv750242



Internal ID15697512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70689573..70690475hg38UCSC Ensembl
Innerchr10:72449329..72450231hg19UCSC Ensembl
Innerchr10:72119335..72120237hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38903
hg19903
hg18903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551485
Supporting Variants
Samples
Known GenesADAMTS14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv750242
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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