A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679417



Internal ID15069383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98408194..98408615hg38UCSC Ensembl
Innerchr10:100167951..100168372hg19UCSC Ensembl
Innerchr10:100157941..100158362hg18UCSC Ensembl
Innerchr10:100157941..100158362hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38422
hg19422
hg18422
hg17422
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515723
Supporting Variants
Samples
Known GenesPYROXD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679417
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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