A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11662491



Internal ID6365217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159778051..159874761hg38UCSC Ensembl
chr4:160699203..160795913hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3896711
hg1996711
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602850
Supporting Variants
SamplesNA20296
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11662491
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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