A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054629



Internal ID19143848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22058630..22221077hg38UCSC Ensembl
Innerchr11:22080176..22242623hg19UCSC Ensembl
Innerchr11:22036752..22199199hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38162448
hg19162448
hg18162448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522738
Samples
Known GenesANO5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054629
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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