A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701683



Internal ID15091649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102380593..102415138hg38UCSC Ensembl
Innerchr10:104140350..104174895hg19UCSC Ensembl
Innerchr10:104130340..104164885hg18UCSC Ensembl
Innerchr10:104130340..104164885hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3834546
hg1934546
hg1834546
hg1734546
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525546
Supporting Variants
Samples
Known GenesGBF1, NFKB2, PSD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701683
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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