A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563435



Internal ID16350844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113997441..114118315hg38UCSC Ensembl
Innerchr13:114762917..114883790hg19UCSC Ensembl
Innerchr13:113781019..113901892hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38120875
hg19120874
hg18120874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820875
Samples
Known GenesRASA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563435
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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