A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596476



Internal ID6636747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68027068..68027902hg38UCSC Ensembl
Innerchr3:68027118..68027852hg38UCSC Ensembl
Outerchr3:68026963..68028007hg38UCSC Ensembl
chr3:68076219..68077053hg19UCSC Ensembl
Innerchr3:68076269..68077003hg19UCSC Ensembl
Outerchr3:68076114..68077158hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38835
hg19835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11031507
SamplesHG04106
Known GenesFAM19A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596476
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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