A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1029098



Internal ID15535598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:37839783..37840305hg38UCSC Ensembl
Innerchr5:37839885..37840407hg19UCSC Ensembl
Innerchr5:37875642..37876164hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38523
hg19523
hg18523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597852
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1029098
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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