A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756073



Internal ID16050029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101277891..101311652hg38UCSC Ensembl
Innerchr10:103037648..103071409hg19UCSC Ensembl
Innerchr10:103027638..103061399hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3833762
hg1933762
hg1833762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552053
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)nssv756073
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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