A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11636632



Internal ID3023338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141581458..141582710hg38UCSC Ensembl
Innerchr4:141581467..141582701hg38UCSC Ensembl
Outerchr4:141581449..141582719hg38UCSC Ensembl
chr4:142502611..142503863hg19UCSC Ensembl
Innerchr4:142502620..142503854hg19UCSC Ensembl
Outerchr4:142502602..142503872hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381253
hg191253
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602468
Supporting Variants
SamplesHG02660
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11636632
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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