A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597038



Internal ID16384447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8702973..8753621hg38UCSC Ensembl
Innerchr5:8703085..8753733hg19UCSC Ensembl
Innerchr5:8756085..8806733hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3850649
hg1950649
hg1850649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9568n54
Supporting Variantsnssv1024006, nssv1024009, nssv1024008, nssv1024007, nssv1024005
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597038
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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