A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597097



Internal ID16384506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9902228..9933108hg38UCSC Ensembl
Innerchr5:9902340..9933220hg19UCSC Ensembl
Innerchr5:9955340..9986220hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3830881
hg1930881
hg1830881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9574n54
Supporting Variantsnssv1153031
Samples1780862015_A
Known GenesLOC285692
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597097
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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