A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11821328



Internal ID3899426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17288872..17298867hg38UCSC Ensembl
Innerchr5:17288872..17298867hg38UCSC Ensembl
Outerchr5:17288808..17298916hg38UCSC Ensembl
chr5:17288981..17298976hg19UCSC Ensembl
Innerchr5:17288981..17298976hg19UCSC Ensembl
Outerchr5:17288917..17299025hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg389996
hg199996
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3604157
Supporting Variants
SamplesHG03557
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11821328
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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