A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174273



Internal ID15876444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121616342..121632864hg38UCSC Ensembl
Innerchr10:123375856..123392378hg19UCSC Ensembl
Innerchr10:123365846..123382368hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3816523
hg1916523
hg1816523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552233
Supporting Variants
SamplesHGDP00841
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174273
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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