A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603907



Internal ID6990938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5737065..5744657hg38UCSC Ensembl
Innerchr5:5737089..5744634hg38UCSC Ensembl
Outerchr5:5737042..5744681hg38UCSC Ensembl
chr5:5737178..5744770hg19UCSC Ensembl
Innerchr5:5737202..5744747hg19UCSC Ensembl
Outerchr5:5737155..5744794hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg387593
hg197593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11799914
SamplesNA20815
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603907
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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