A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563431



Internal ID16350840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113976420..114033126hg38UCSC Ensembl
Innerchr13:114745831..114798602hg19UCSC Ensembl
Innerchr13:113763933..113816704hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3856707
hg1952772
hg1852772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3458n54
Supporting Variantsnssv820871
Samples
Known GenesRASA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563431
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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