A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv598549



Internal ID16385958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:70922561..70941301hg38UCSC Ensembl
Innerchr5:70218388..70237128hg19UCSC Ensembl
Innerchr5:70254144..70272884hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3818741
hg1918741
hg1818741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9858n54
Supporting Variantsnssv1034931
Samples
Known GenesSMN1, SMN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv598549
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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