A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510753



Internal ID18809034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37798154..37909925hg38UCSC Ensembl
Innerchr11:37819704..37931475hg19UCSC Ensembl
Innerchr11:37776280..37888051hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38111772
hg19111772
hg18111772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048290
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)nssv3510753
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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