A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637556



Internal ID6677660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:204376..215336hg38UCSC Ensembl
Innerchr16:204376..215336hg38UCSC Ensembl
Outerchr16:203876..215836hg38UCSC Ensembl
chr16:254375..265335hg19UCSC Ensembl
Innerchr16:254375..265335hg19UCSC Ensembl
Outerchr16:253875..265835hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810961
hg1910961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15355150
SamplesNA19786
Known GenesLUC7L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637556
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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