A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599925



Internal ID16387334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:143013997..143036550hg38UCSC Ensembl
Innerchr5:142393562..142416115hg19UCSC Ensembl
Innerchr5:142373755..142396308hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3822554
hg1922554
hg1822554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1042428
Samples
Known GenesARHGAP26
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599925
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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