A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037743



Internal ID19126962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:100627978..100650312hg38UCSC Ensembl
Innerchr11:100498709..100521043hg19UCSC Ensembl
Innerchr11:100003919..100026253hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3822335
hg1922335
hg1822335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504261
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)nsv1037743
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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