A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035762



Internal ID19124981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4215479..4315287hg38UCSC Ensembl
Innerchr11:4236709..4336517hg19UCSC Ensembl
Innerchr11:4193285..4293093hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3899809
hg1999809
hg1899809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1020n100
Supporting Variantsnssv3504117
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)nsv1035762
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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