A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599076



Internal ID16386485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98087772..98142851hg38UCSC Ensembl
Innerchr5:97423476..97478555hg19UCSC Ensembl
Innerchr5:97449232..97504311hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3855080
hg1955080
hg1855080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1038759, nssv1038758
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599076
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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