A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597039



Internal ID16384448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702973..8757578hg38UCSC Ensembl
Innerchr5:8703085..8757690hg19UCSC Ensembl
Innerchr5:8756085..8810690hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3854606
hg1954606
hg1854606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9568n54
Supporting Variantsnssv1024010
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597039
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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