A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893656



Internal ID19184476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4051127..4068463hg38UCSC Ensembl
Outerchr1:4051127..4068463hg38UCSC Ensembl
Innerchr1:4111187..4128523hg19UCSC Ensembl
Outerchr1:4111187..4128523hg19UCSC Ensembl
Innerchr1:4011047..4028383hg18UCSC Ensembl
Outerchr1:4011047..4028383hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3817337
hg1917337
hg1817337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779899
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893656
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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