A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527554



Internal ID15108161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:123687422..123688189hg38UCSC Ensembl
Innerchr10:125446938..125447705hg19UCSC Ensembl
Innerchr10:125436928..125437695hg18UCSC Ensembl
Innerchr10:125436928..125437695hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38768
hg19768
hg18768
hg17768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704015
Samples
Known GenesGPR26
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527554
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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