A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891896



Internal ID19186292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126281817..127117455hg38UCSC Ensembl
Outerchr10:126281817..127117455hg38UCSC Ensembl
Innerchr10:127970386..128915719hg19UCSC Ensembl
Outerchr10:127970386..128915719hg19UCSC Ensembl
Innerchr10:127960376..128805709hg18UCSC Ensembl
Outerchr10:127960376..128805709hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38835639
hg19945334
hg18845334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790766
Samples
Known GenesADAM12, C10orf90, DOCK1, LINC00601
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891896
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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