A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv761957



Internal ID16055913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132505349..132522229hg38UCSC Ensembl
Innerchr10:134318853..134335733hg19UCSC Ensembl
Innerchr10:134168843..134185723hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3816881
hg1916881
hg1816881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552520
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv761957
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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