A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600251



Internal ID6640515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37877712..37879870hg38UCSC Ensembl
Innerchr4:37877764..37879819hg38UCSC Ensembl
Outerchr4:37877661..37879922hg38UCSC Ensembl
chr4:37879333..37881491hg19UCSC Ensembl
Innerchr4:37879385..37881440hg19UCSC Ensembl
Outerchr4:37879282..37881543hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382159
hg192159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11396052, essv11396053
SamplesHG03079, NA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600251
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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