A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053083



Internal ID19142302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81274905..81304079hg38UCSC Ensembl
Innerchr11:80985948..81015122hg19UCSC Ensembl
Innerchr11:80663596..80692770hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3829175
hg1929175
hg1829175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1241n100
Supporting Variantsnssv3506528, nssv3505720
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)nsv1053083
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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