A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597610



Internal ID16385019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25302874..25390972hg38UCSC Ensembl
Innerchr5:25302983..25391081hg19UCSC Ensembl
Innerchr5:25338740..25426838hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3888099
hg1988099
hg1888099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153041
Samples1798860592_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597610
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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