A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778863



Internal ID19176582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126976608..127048956hg38UCSC Ensembl
Innerchr10:128774872..128847220hg19UCSC Ensembl
Innerchr10:128664862..128737210hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3872349
hg1972349
hg1872349
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891897
Supporting Variants
Samples
Known GenesDOCK1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778863
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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