A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597301



Internal ID6637571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107127962..107129339hg38UCSC Ensembl
Innerchr3:107127962..107129339hg38UCSC Ensembl
Outerchr3:107127652..107129574hg38UCSC Ensembl
chr3:106846809..106848186hg19UCSC Ensembl
Innerchr3:106846809..106848186hg19UCSC Ensembl
Outerchr3:106846499..106848421hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg381378
hg191378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11094680
SamplesHG00524
Known GenesLINC00882
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597301
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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