A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603476



Internal ID6990507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184845973..184847972hg38UCSC Ensembl
Innerchr4:184845986..184847959hg38UCSC Ensembl
Outerchr4:184845960..184847985hg38UCSC Ensembl
chr4:185767127..185769126hg19UCSC Ensembl
Innerchr4:185767140..185769113hg19UCSC Ensembl
Outerchr4:185767114..185769139hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11734120
SamplesNA19030
Known GenesLOC731424
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603476
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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