A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043937



Internal ID19133156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21589423..21692904hg38UCSC Ensembl
Innerchr11:21610969..21714450hg19UCSC Ensembl
Innerchr11:21567545..21671026hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38103482
hg19103482
hg18103482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507490
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)nsv1043937
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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