A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596795



Internal ID6984109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:83568742..83725205hg38UCSC Ensembl
Innerchr3:83568742..83725205hg38UCSC Ensembl
Outerchr3:83568242..83725705hg38UCSC Ensembl
chr3:83617893..83774356hg19UCSC Ensembl
Innerchr3:83617893..83774356hg19UCSC Ensembl
Outerchr3:83617393..83774856hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38156464
hg19156464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11058813
SamplesHG02052
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596795
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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