A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11661824



Internal ID5641859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159389896..159391660hg38UCSC Ensembl
Innerchr4:159389905..159391651hg38UCSC Ensembl
Outerchr4:159389887..159391669hg38UCSC Ensembl
chr4:160311048..160312812hg19UCSC Ensembl
Innerchr4:160311057..160312803hg19UCSC Ensembl
Outerchr4:160311039..160312821hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381765
hg191765
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602845
Supporting Variants
SamplesNA19063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11661824
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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