A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043964



Internal ID18786495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76158693..76191164hg38UCSC Ensembl
Innerchr11:75869737..75902208hg19UCSC Ensembl
Innerchr11:75547385..75579856hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3832472
hg1932472
hg1832472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1226n100
Supporting Variantsnssv3510471, nssv3520349
Samples
Known GenesWNT11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043964
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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