A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11394324



Internal ID436123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35821118..35840242hg38UCSC Ensembl
Innerchr4:35821145..35840215hg38UCSC Ensembl
Outerchr4:35821091..35840269hg38UCSC Ensembl
chr4:35822740..35841864hg19UCSC Ensembl
Innerchr4:35822767..35841837hg19UCSC Ensembl
Outerchr4:35822713..35841891hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3819125
hg1919125
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600207
Supporting Variants
SamplesHG00133
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11394324
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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