A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786914



Internal ID18828635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12080356..12104859hg38UCSC Ensembl
Innerchr10:12122355..12146858hg19UCSC Ensembl
Innerchr10:12162361..12186864hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3824504
hg1924504
hg1824504
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891755
Supporting Variants
Samples
Known GenesDHTKD1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786914
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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