A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521910



Internal ID15102517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:114440380..114446139hg38UCSC Ensembl
Innerchr7:114080435..114086194hg19UCSC Ensembl
Innerchr7:113867671..113873430hg18UCSC Ensembl
Innerchr7:113674386..113680145hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg385760
hg195760
hg185760
hg175760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694681
Samples
Known GenesFOXP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521910
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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