A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598949



Internal ID16039672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:93584409..93587075hg38UCSC Ensembl
Innerchr5:92920115..92922781hg19UCSC Ensembl
Innerchr5:92945871..92948537hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg382667
hg192667
hg182667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1038094
Samples
Known GenesNR2F1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598949
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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