A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174562



Internal ID15853685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84680093..84703258hg38UCSC Ensembl
Innerchr10:86439849..86463014hg19UCSC Ensembl
Innerchr10:86429829..86452994hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3823166
hg1923166
hg1823166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551757
Supporting Variants
Samples1780854340_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174562
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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