A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11385979



Internal ID4088679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31570313..31580741hg38UCSC Ensembl
Innerchr4:31570313..31580741hg38UCSC Ensembl
Outerchr4:31570177..31580875hg38UCSC Ensembl
chr4:31571935..31582363hg19UCSC Ensembl
Innerchr4:31571935..31582363hg19UCSC Ensembl
Outerchr4:31571799..31582497hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3810429
hg1910429
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600095
Supporting Variants
SamplesHG03716
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11385979
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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