A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603923



Internal ID6990954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7093168..7115566hg38UCSC Ensembl
Innerchr5:7093168..7115566hg38UCSC Ensembl
Outerchr5:7093034..7115673hg38UCSC Ensembl
chr5:7093281..7115679hg19UCSC Ensembl
Innerchr5:7093281..7115679hg19UCSC Ensembl
Outerchr5:7093147..7115786hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3822399
hg1922399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11802118
SamplesHG03803
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603923
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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