A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519632



Internal ID18817913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28951610..28992762hg38UCSC Ensembl
Innerchr11:28973157..29014309hg19UCSC Ensembl
Innerchr11:28929733..28970885hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3841153
hg1941153
hg1841153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048813
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)nssv3519632
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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