A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637569



Internal ID6677673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:320893..377048hg38UCSC Ensembl
chr16:370893..427048hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3856156
hg1956156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15355217
SamplesHG00629
Known GenesAXIN1, MRPL28, TMEM8A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637569
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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