A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747040



Internal ID16040996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38782022..38847294hg38UCSC Ensembl
Innerchr10:39075153..39140425hg19UCSC Ensembl
Innerchr10:39115159..39180431hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3865273
hg1965273
hg1865273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550544
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)nssv747040
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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