A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3708514



Internal ID19006795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8281916..8302999hg38UCSC Ensembl
Innerchr11:8303463..8324546hg19UCSC Ensembl
Innerchr11:8260039..8281122hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3821084
hg1921084
hg1821084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036104
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)nssv3708514
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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