A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786976



Internal ID19180803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26602511..26654988hg38UCSC Ensembl
Innerchr1:26929002..26981479hg19UCSC Ensembl
Innerchr1:26801589..26854066hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3852478
hg1952478
hg1852478
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893192
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786976
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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