A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518656



Internal ID18470251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31525320..31593772hg38UCSC Ensembl
Innerchr11:31546867..31615319hg19UCSC Ensembl
Innerchr11:31503443..31571895hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3868453
hg1968453
hg1868453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047475
Supporting Variants
Samples
Known GenesELP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3518656
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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