A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596507



Internal ID6983822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70007261..70016356hg38UCSC Ensembl
Innerchr3:70007411..70016206hg38UCSC Ensembl
Outerchr3:70007111..70016506hg38UCSC Ensembl
chr3:70056412..70065507hg19UCSC Ensembl
Innerchr3:70056562..70065357hg19UCSC Ensembl
Outerchr3:70056262..70065657hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg389096
hg199096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11038149, essv11038146, essv11038150, essv11038148, essv11038147
SamplesHG02852, NA19239, NA20318, NA19749, NA20289
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596507
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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