A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598928



Internal ID16386337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:90954083..91002815hg38UCSC Ensembl
Innerchr5:90249900..90298632hg19UCSC Ensembl
Innerchr5:90285656..90334388hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3848733
hg1948733
hg1848733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9934n54
Supporting Variantsnssv1153045
Samples1780854061_A
Known GenesGPR98
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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