A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv758783



Internal ID16052739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114025486..114040878hg38UCSC Ensembl
Innerchr10:115785245..115800637hg19UCSC Ensembl
Innerchr10:115775235..115790627hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3815393
hg1915393
hg1815393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552202
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)nssv758783
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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