A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587115



Internal ID6627422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107826748..107827377hg38UCSC Ensembl
Innerchr1:107826748..107827377hg38UCSC Ensembl
Outerchr1:107826536..107827583hg38UCSC Ensembl
chr1:108369370..108369999hg19UCSC Ensembl
Innerchr1:108369370..108369999hg19UCSC Ensembl
Outerchr1:108369158..108370205hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10051526, essv10051527
SamplesNA18612, HG00729
Known GenesVAV3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587115
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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