A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11660041



Internal ID5885365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157699145..157722092hg38UCSC Ensembl
Innerchr4:157699645..157721592hg38UCSC Ensembl
Outerchr4:157698145..157723092hg38UCSC Ensembl
chr4:158620297..158643244hg19UCSC Ensembl
Innerchr4:158620797..158642744hg19UCSC Ensembl
Outerchr4:158619297..158644244hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3822948
hg1922948
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602817
Supporting Variants
SamplesNA19310
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11660041
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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