A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597732



Internal ID16385141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28806149..28986843hg38UCSC Ensembl
Innerchr5:28806256..28986950hg19UCSC Ensembl
Innerchr5:28842013..29022707hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38180695
hg19180695
hg18180695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9710n54
Supporting Variantsnssv1028730, nssv1028731, nssv1028729
Samples
Known GenesLSP1P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597732
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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