A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11375571



Internal ID5003430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26441158..26452552hg38UCSC Ensembl
Innerchr4:26441158..26452552hg38UCSC Ensembl
Outerchr4:26440833..26452858hg38UCSC Ensembl
chr4:26442780..26454174hg19UCSC Ensembl
Innerchr4:26442780..26454174hg19UCSC Ensembl
Outerchr4:26442455..26454480hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3811395
hg1911395
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599987
Supporting Variants
SamplesNA18504
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11375571
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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