A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524438



Internal ID15105045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:114223329..114242862hg38UCSC Ensembl
Innerchr7:113863384..113882917hg19UCSC Ensembl
Innerchr7:113650620..113670153hg18UCSC Ensembl
Innerchr7:113457335..113476868hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3819534
hg1919534
hg1819534
hg1719534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700368
Samples
Known GenesFOXP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524438
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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