A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523003



Internal ID15103610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48709016..48712563hg38UCSC Ensembl
Innerchr10:49917061..49920608hg19UCSC Ensembl
Innerchr10:49587067..49590614hg18UCSC Ensembl
Innerchr10:49587067..49590614hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg383548
hg193548
hg183548
hg173548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698675
Samples
Known GenesWDFY4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523003
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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