A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526764



Internal ID15454057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103061379..103096804hg38UCSC Ensembl
Innerchr7:102701826..102737251hg19UCSC Ensembl
Innerchr7:102489062..102524487hg18UCSC Ensembl
Innerchr7:102295777..102331202hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3835426
hg1935426
hg1835426
hg1735426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703116
Samples
Known GenesARMC10, FBXL13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526764
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer