A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11396053



Internal ID1397869
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600251
Supporting Variants
SamplesNA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11396053
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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