A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv970928



Internal ID16264884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103461553..103589916hg38UCSC Ensembl
Innerchr3:103180397..103308760hg19UCSC Ensembl
Innerchr3:104663087..104791450hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38128364
hg19128364
hg18128364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591201
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)nssv970928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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