A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv750260



Internal ID16044216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70964109..70986625hg38UCSC Ensembl
Innerchr10:72723866..72746382hg19UCSC Ensembl
Innerchr10:72393872..72416388hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3822517
hg1922517
hg1822517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551498
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)nssv750260
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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