A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523484



Internal ID15104091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128103129..128106653hg38UCSC Ensembl
Innerchr10:129901393..129904917hg19UCSC Ensembl
Innerchr10:129791383..129794907hg18UCSC Ensembl
Innerchr10:129791383..129794907hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg383525
hg193525
hg183525
hg173525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699250
Samples
Known GenesMKI67
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523484
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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