A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782126



Internal ID18827849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19760441..19779641hg38UCSC Ensembl
Innerchr19:19871250..19890450hg19UCSC Ensembl
Innerchr19:19732250..19751450hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3819201
hg1919201
hg1819201
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893168
Supporting Variants
Samples
Known GenesLINC00663
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782126
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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