A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891897



Internal ID19186293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126976608..127048956hg38UCSC Ensembl
Outerchr10:126976608..127048956hg38UCSC Ensembl
Innerchr10:128774872..128847220hg19UCSC Ensembl
Outerchr10:128774872..128847220hg19UCSC Ensembl
Innerchr10:128664862..128737210hg18UCSC Ensembl
Outerchr10:128664862..128737210hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3872349
hg1972349
hg1872349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778863
Samples
Known GenesDOCK1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891897
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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