A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11677906



Internal ID3810115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:164883831..164902963hg38UCSC Ensembl
chr4:165804983..165824115hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3819133
hg1919133
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603007
Supporting Variants
SamplesHG03452
Known GenesLOC100506013
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11677906
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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