A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11026522



Internal ID1028338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62678720..62709990hg38UCSC Ensembl
Innerchr3:62678870..62709840hg38UCSC Ensembl
Outerchr3:62678570..62710140hg38UCSC Ensembl
chr3:62664395..62695665hg19UCSC Ensembl
Innerchr3:62664545..62695515hg19UCSC Ensembl
Outerchr3:62664245..62695815hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3831271
hg1931271
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596377
Supporting Variants
SamplesNA18505
Known GenesCADPS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11026522
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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