A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780095



Internal ID19177935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57811677..58008290hg38UCSC Ensembl
Innerchr10:59571437..59768050hg19UCSC Ensembl
Innerchr10:59241443..59438056hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38196614
hg19196614
hg18196614
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891830
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=57
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780095
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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