A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598961



Internal ID16039684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:95807113..95832451hg38UCSC Ensembl
Innerchr5:95142817..95168155hg19UCSC Ensembl
Innerchr5:95168573..95193911hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3825339
hg1925339
hg1825339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153052
SamplesNINDS_229
Known GenesGLRX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598961
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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