A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521787



Internal ID15102394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28169973..28175824hg38UCSC Ensembl
Innerchr10:28458902..28464753hg19UCSC Ensembl
Innerchr10:28498908..28504759hg18UCSC Ensembl
Innerchr10:28498908..28504759hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg385852
hg195852
hg185852
hg175852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694555
Samples
Known GenesMPP7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521787
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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