A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11587871



Internal ID6482529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120197935..120303644hg38UCSC Ensembl
Innerchr4:120197975..120303604hg38UCSC Ensembl
Outerchr4:120197895..120303684hg38UCSC Ensembl
chr4:121119090..121224799hg19UCSC Ensembl
Innerchr4:121119130..121224759hg19UCSC Ensembl
Outerchr4:121119050..121224839hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38105710
hg19105710
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601988
Supporting Variants
SamplesNA20525
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11587871
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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