A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700368



Internal ID15437020
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524438
Supporting Variants
Samples
Known GenesFOXP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700368
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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