A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891755



Internal ID18839465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12080356..12104859hg38UCSC Ensembl
Outerchr10:12080356..12104859hg38UCSC Ensembl
Innerchr10:12122355..12146858hg19UCSC Ensembl
Outerchr10:12122355..12146858hg19UCSC Ensembl
Innerchr10:12162361..12186864hg18UCSC Ensembl
Outerchr10:12162361..12186864hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3824504
hg1924504
hg1824504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786914
Samples
Known GenesDHTKD1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891755
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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