A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638740



Internal ID7025525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59092610..59100772hg38UCSC Ensembl
Innerchr16:59092610..59100772hg38UCSC Ensembl
Outerchr16:59092370..59101009hg38UCSC Ensembl
chr16:59126514..59134676hg19UCSC Ensembl
Innerchr16:59126514..59134676hg19UCSC Ensembl
Outerchr16:59126274..59134913hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg388163
hg198163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15492240
SamplesHG02759
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638740
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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