A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600026



Internal ID16040749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151411076..151414457hg38UCSC Ensembl
Innerchr5:150790637..150794018hg19UCSC Ensembl
Innerchr5:150770830..150774211hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg383382
hg193382
hg183382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10124n54
Supporting Variantsnssv1043699, nssv1043700
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600026
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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