A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151921



Internal ID15881122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65199224..65230129hg38UCSC Ensembl
Innerchr3:65184899..65215804hg19UCSC Ensembl
Innerchr3:65159939..65190844hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3830906
hg1930906
hg1830906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590483
Supporting Variants
SamplesNINDS_70
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151921
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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