A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562783



Internal ID16003506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96090029..96090785hg38UCSC Ensembl
Innerchr13:96742283..96743039hg19UCSC Ensembl
Innerchr13:95540284..95541040hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38757
hg19757
hg18757
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3329n54
Supporting Variantsnssv817552, nssv817555, nssv817553, nssv817554, nssv817551, nssv817557, nssv817556
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562783
Frequency
Sample Size17421
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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