A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151348



Internal ID15880407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:193014190..193271097hg38UCSC Ensembl
Innerchr2:193878916..194135822hg19UCSC Ensembl
Innerchr2:193587161..193844067hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38256908
hg19256907
hg18256907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584072
Supporting Variants
SamplesNINDS_206
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151348
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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