A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600878



Internal ID6987917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68730910..68805645hg38UCSC Ensembl
Innerchr4:68730921..68805634hg38UCSC Ensembl
Outerchr4:68730899..68805656hg38UCSC Ensembl
chr4:69596628..69671363hg19UCSC Ensembl
Innerchr4:69596639..69671352hg19UCSC Ensembl
Outerchr4:69596617..69671374hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3874736
hg1974736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11485266
SamplesNA19914
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600878
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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