A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598368



Internal ID16385777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:64402581..64412561hg38UCSC Ensembl
Innerchr5:63698408..63708388hg19UCSC Ensembl
Innerchr5:63734164..63744144hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg389981
hg199981
hg189981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1034528, nssv1034529
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598368
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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