A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037670



Internal ID18780201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76158391..76245304hg38UCSC Ensembl
Innerchr11:75869435..75956348hg19UCSC Ensembl
Innerchr11:75547083..75633996hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3886914
hg1986914
hg1886914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1227n100
Supporting Variantsnssv3505238
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)nsv1037670
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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