A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603927



Internal ID6990958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7167356..7176615hg38UCSC Ensembl
Innerchr5:7167356..7176615hg38UCSC Ensembl
Outerchr5:7167269..7176761hg38UCSC Ensembl
chr5:7167469..7176728hg19UCSC Ensembl
Innerchr5:7167469..7176728hg19UCSC Ensembl
Outerchr5:7167382..7176874hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg389260
hg199260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11802869, essv11802868, essv11802871, essv11802870
SamplesHG00422, HG00629, NA18535, NA18943
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603927
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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