A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747183



Internal ID16041139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:41813135..41861510hg38UCSC Ensembl
Innerchr10:42378699..42427074hg19UCSC Ensembl
Innerchr10:41698705..41747080hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3848376
hg1948376
hg1848376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550607
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)nssv747183
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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