A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11690426



Internal ID5317406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169877462..169882167hg38UCSC Ensembl
Innerchr4:169877472..169882157hg38UCSC Ensembl
Outerchr4:169877452..169882177hg38UCSC Ensembl
chr4:170798613..170803318hg19UCSC Ensembl
Innerchr4:170798623..170803308hg19UCSC Ensembl
Outerchr4:170798603..170803328hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg384706
hg194706
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603130
Supporting Variants
SamplesNA18865
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11690426
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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