A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894100



Internal ID19184954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5673953..5710205hg38UCSC Ensembl
Outerchr1:5673953..5710205hg38UCSC Ensembl
Innerchr1:5734013..5770265hg19UCSC Ensembl
Outerchr1:5734013..5770265hg19UCSC Ensembl
Innerchr1:5656600..5692852hg18UCSC Ensembl
Outerchr1:5656600..5692852hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3836253
hg1936253
hg1836253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798932
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894100
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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