A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597139



Internal ID16384548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10699378..10743817hg38UCSC Ensembl
Innerchr5:10699490..10743929hg19UCSC Ensembl
Innerchr5:10752490..10796929hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3844440
hg1944440
hg1844440
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1025276
Samples
Known GenesDAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597139
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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