A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596632



Internal ID6983946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:76295328..76296200hg38UCSC Ensembl
Innerchr3:76295378..76296150hg38UCSC Ensembl
Outerchr3:76295275..76296253hg38UCSC Ensembl
chr3:76344479..76345351hg19UCSC Ensembl
Innerchr3:76344529..76345301hg19UCSC Ensembl
Outerchr3:76344426..76345404hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11046823
SamplesHG01528
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596632
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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