A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043737



Internal ID19132956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:129573237..129648597hg38UCSC Ensembl
Innerchr11:129443132..129518492hg19UCSC Ensembl
Innerchr11:128948342..129023702hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3875361
hg1975361
hg1875361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507288
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)nsv1043737
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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