A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890682



Internal ID18838298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:156899922..156951428hg38UCSC Ensembl
Outerchr1:156899922..156951428hg38UCSC Ensembl
Innerchr1:156869714..156921220hg19UCSC Ensembl
Outerchr1:156869714..156921220hg19UCSC Ensembl
Innerchr1:155136338..155187844hg18UCSC Ensembl
Outerchr1:155136338..155187844hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3851507
hg1951507
hg1851507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797707
Samples
Known GenesARHGEF11, LRRC71, MIR765, PEAR1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890682
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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