A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600658



Internal ID16388067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179494860..179523813hg38UCSC Ensembl
Innerchr5:178921861..178950814hg19UCSC Ensembl
Innerchr5:178854467..178883420hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3828954
hg1928954
hg1828954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1047021
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600658
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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