A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702994



Internal ID15092960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102363085..102397954hg38UCSC Ensembl
Innerchr10:104122842..104157711hg19UCSC Ensembl
Innerchr10:104112832..104147701hg18UCSC Ensembl
Innerchr10:104112832..104147701hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3834870
hg1934870
hg1834870
hg1734870
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526665
Supporting Variants
Samples
Known GenesGBF1, NFKB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702994
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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