A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695662



Internal ID15432314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87753082..87824245hg38UCSC Ensembl
Innerchr10:89512839..89584002hg19UCSC Ensembl
Innerchr10:89502819..89573982hg18UCSC Ensembl
Innerchr10:89502819..89573982hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3871164
hg1971164
hg1871164
hg1771164
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518233
Supporting Variants
Samples
Known GenesATAD1, CFL1P1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695662
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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