A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11078865



Internal ID4407598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99052037..99180176hg38UCSC Ensembl
chr3:98770881..98899020hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38128140
hg19128140
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597129
Supporting Variants
SamplesHG03922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11078865
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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