A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528026



Internal ID15108633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13227931..13233643hg38UCSC Ensembl
Innerchr10:13269931..13275643hg19UCSC Ensembl
Innerchr10:13309937..13315649hg18UCSC Ensembl
Innerchr10:13309937..13315649hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385713
hg195713
hg185713
hg175713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704555
Samples
Known GenesUCMA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528026
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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