A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749782



Internal ID16043738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65700336..65881443hg38UCSC Ensembl
Innerchr10:67460094..67641201hg19UCSC Ensembl
Innerchr10:67130100..67311207hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38181108
hg19181108
hg18181108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551294
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)nssv749782
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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