A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11747377



Internal ID6138359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186824735..186837851hg38UCSC Ensembl
Innerchr4:186824735..186837851hg38UCSC Ensembl
Outerchr4:186824235..186838351hg38UCSC Ensembl
chr4:187745889..187759005hg19UCSC Ensembl
Innerchr4:187745889..187759005hg19UCSC Ensembl
Outerchr4:187745389..187759505hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3813117
hg1913117
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603541
Supporting Variants
SamplesNA19670
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11747377
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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