A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710741



Internal ID19009022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106176123..106204296hg38UCSC Ensembl
Innerchr11:106046850..106075023hg19UCSC Ensembl
Innerchr11:105552060..105580233hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3828174
hg1928174
hg1828174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036986
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)nssv3710741
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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