A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563126



Internal ID16350535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110676272..110677948hg38UCSC Ensembl
Innerchr13:111328619..111330295hg19UCSC Ensembl
Innerchr13:110126620..110128296hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381677
hg191677
hg181677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3396n54
Supporting Variantsnssv819760
Samples
Known GenesCARS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563126
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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