A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596768



Internal ID6984082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82419296..82424400hg38UCSC Ensembl
Innerchr3:82419296..82424400hg38UCSC Ensembl
Outerchr3:82419271..82424580hg38UCSC Ensembl
chr3:82468447..82473551hg19UCSC Ensembl
Innerchr3:82468447..82473551hg19UCSC Ensembl
Outerchr3:82468422..82473731hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg385105
hg195105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11055449
SamplesHG03890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596768
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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