A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174624



Internal ID15853592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38227656..38294034hg38UCSC Ensembl
Innerchr11:38249206..38315584hg19UCSC Ensembl
Innerchr11:38205782..38272160hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3866379
hg1966379
hg1866379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554033
Supporting Variants
Samples1780854299_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174624
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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