A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676229



Internal ID15066195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1156508..1178396hg38UCSC Ensembl
Innerchr10:1202448..1224336hg19UCSC Ensembl
Innerchr10:1192448..1214336hg18UCSC Ensembl
Innerchr10:1192448..1214336hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3821889
hg1921889
hg1821889
hg1721889
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517780
Supporting Variants
Samples
Known GenesADARB2, LINC00200
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676229
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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