A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517145



Internal ID18815426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25112285..25275385hg38UCSC Ensembl
Innerchr11:25133831..25296931hg19UCSC Ensembl
Innerchr11:25090407..25253507hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38163101
hg19163101
hg18163101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049506
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)nssv3517145
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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