A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782838



Internal ID19159870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105491704..105698010hg38UCSC Ensembl
Innerchr1:106034326..106240632hg19UCSC Ensembl
Innerchr1:105835849..106042155hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38206307
hg19206307
hg18206307
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893923
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=46
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782838
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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