A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599957



Internal ID16040680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:150402561..150407327hg38UCSC Ensembl
Innerchr5:149782124..149786890hg19UCSC Ensembl
Innerchr5:149762317..149767083hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg384767
hg194767
hg184767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1043283
Samples
Known GenesCD74
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599957
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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