A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637557



Internal ID6677661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:223141..224750hg38UCSC Ensembl
Innerchr16:223141..224750hg38UCSC Ensembl
Outerchr16:223064..224793hg38UCSC Ensembl
chr16:273140..274749hg19UCSC Ensembl
Innerchr16:273140..274749hg19UCSC Ensembl
Outerchr16:273063..274792hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381610
hg191610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15355153, essv15355152, essv15355151
SamplesHG00355, HG00737, NA06984
Known GenesLUC7L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637557
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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