A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892747



Internal ID19183567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21626943..21643796hg38UCSC Ensembl
Outerchr1:21626943..21643796hg38UCSC Ensembl
Innerchr1:21953436..21970289hg19UCSC Ensembl
Outerchr1:21953436..21970289hg19UCSC Ensembl
Innerchr1:21826023..21842876hg18UCSC Ensembl
Outerchr1:21826023..21842876hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3816854
hg1916854
hg1816854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780387
Samples
Known GenesRAP1GAP
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892747
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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