A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893756



Internal ID19184576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79693536..79779067hg38UCSC Ensembl
Outerchr1:79693536..79779067hg38UCSC Ensembl
Innerchr1:80159221..80244752hg19UCSC Ensembl
Outerchr1:80159221..80244752hg19UCSC Ensembl
Innerchr1:79931809..80017340hg18UCSC Ensembl
Outerchr1:79931809..80017340hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3885532
hg1985532
hg1885532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780403
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893756
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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