A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152025



Internal ID15880694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162412903..162510082hg38UCSC Ensembl
Innerchr3:162130691..162227870hg19UCSC Ensembl
Innerchr3:163613385..163710564hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3897180
hg1997180
hg1897180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592176
Supporting Variants
SamplesNINDS_249
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152025
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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