A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524427



Internal ID15105034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:98408615..98452617hg38UCSC Ensembl
Innerchr10:100168372..100212374hg19UCSC Ensembl
Innerchr10:100158362..100202364hg18UCSC Ensembl
Innerchr10:100158362..100202364hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3844003
hg1944003
hg1844003
hg1744003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700354
Samples
Known GenesHPS1, MIR4685, PYROXD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524427
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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