A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616422



Internal ID7003309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16021420..16139525hg38UCSC Ensembl
chr8:15878929..15997034hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38118106
hg19118106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13118963, essv13118964
SamplesHG00337, HG02687
Known GenesMSR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616422
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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