A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796798



Internal ID19161976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:191689020..191788978hg38UCSC Ensembl
Innerchr1:191658150..191758108hg19UCSC Ensembl
Innerchr1:189924773..190024731hg18UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3899959
hg1999959
hg1899959
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890948
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796798
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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