A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598679



Internal ID16039402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:76528140..76618904hg38UCSC Ensembl
Innerchr5:75823965..75914729hg19UCSC Ensembl
Innerchr5:75859721..75950485hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3890765
hg1990765
hg1890765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9884n54
Supporting Variantsnssv1035140
Samples
Known GenesF2RL2, IQGAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598679
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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