A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519437



Internal ID18817718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37319835..37360412hg38UCSC Ensembl
Innerchr11:37341385..37381962hg19UCSC Ensembl
Innerchr11:37297961..37338538hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3840578
hg1940578
hg1840578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050145
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3519437
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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