A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589181



Internal ID6972116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234856883..234868059hg38UCSC Ensembl
Innerchr1:234856933..234868009hg38UCSC Ensembl
Outerchr1:234856771..234868171hg38UCSC Ensembl
chr1:234992630..235003806hg19UCSC Ensembl
Innerchr1:234992680..235003756hg19UCSC Ensembl
Outerchr1:234992518..235003918hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3811177
hg1911177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10331753
SamplesNA20511
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589181
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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