A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637567



Internal ID7024359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:300040..319624hg38UCSC Ensembl
chr16:350040..369624hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819585
hg1919585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15355215, essv15355212, essv15355211, essv15355214, essv15355210, essv15355213
SamplesHG00634, HG00610, HG00629, HG00266, HG00596, NA12272
Known GenesAXIN1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637567
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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