A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604617



Internal ID6991645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32628127..32630641hg38UCSC Ensembl
Innerchr5:32628155..32630614hg38UCSC Ensembl
Outerchr5:32628100..32630669hg38UCSC Ensembl
chr5:32628233..32630747hg19UCSC Ensembl
Innerchr5:32628261..32630720hg19UCSC Ensembl
Outerchr5:32628206..32630775hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg382515
hg192515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11857150
SamplesHG03559
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604617
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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