A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11388173



Internal ID4630064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32648156..32822371hg38UCSC Ensembl
chr4:32649778..32823993hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38174216
hg19174216
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600120
Supporting Variants
SamplesHG04161
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11388173
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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