A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607432



Internal ID6994366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162706535..162716046hg38UCSC Ensembl
Innerchr5:162706564..162716017hg38UCSC Ensembl
Outerchr5:162706506..162716075hg38UCSC Ensembl
chr5:162133541..162143052hg19UCSC Ensembl
Innerchr5:162133570..162143023hg19UCSC Ensembl
Outerchr5:162133512..162143081hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg389512
hg199512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12120191
SamplesNA19026
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607432
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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