A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562784



Internal ID16003507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96090029..96090868hg38UCSC Ensembl
Innerchr13:96742283..96743122hg19UCSC Ensembl
Innerchr13:95540284..95541123hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38840
hg19840
hg18840
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3329n54
Supporting Variantsnssv817561, nssv817560, nssv817558, nssv817562, nssv817559
Samples
Known GenesHS6ST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562784
Frequency
Sample Size17421
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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