A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1038456



Internal ID15891642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97922915..98094823hg38UCSC Ensembl
Innerchr5:97258619..97430527hg19UCSC Ensembl
Innerchr5:97284375..97456283hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38171909
hg19171909
hg18171909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599062
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)nssv1038456
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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