A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037718



Internal ID19126937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4215479..4337814hg38UCSC Ensembl
Innerchr11:4236709..4359044hg19UCSC Ensembl
Innerchr11:4193285..4315620hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38122336
hg19122336
hg18122336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1020n100
Supporting Variantsnssv3505301
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)nsv1037718
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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