A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596449



Internal ID6983764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67125024..67128138hg38UCSC Ensembl
Innerchr3:67125024..67128138hg38UCSC Ensembl
Outerchr3:67124784..67128383hg38UCSC Ensembl
chr3:67175448..67178562hg19UCSC Ensembl
Innerchr3:67175448..67178562hg19UCSC Ensembl
Outerchr3:67175208..67178807hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg383115
hg193115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11030921
SamplesNA12717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596449
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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