A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891855



Internal ID18839565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69199740..69250619hg38UCSC Ensembl
Outerchr10:69199740..69250619hg38UCSC Ensembl
Innerchr10:70959496..71010375hg19UCSC Ensembl
Outerchr10:70959496..71010375hg19UCSC Ensembl
Innerchr10:70629502..70680381hg18UCSC Ensembl
Outerchr10:70629502..70680381hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3850880
hg1950880
hg1850880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787666
Samples
Known GenesHKDC1, SUPV3L1
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891855
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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