A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638781



Internal ID6678878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61638941..61644346hg38UCSC Ensembl
Innerchr16:61638941..61644346hg38UCSC Ensembl
Outerchr16:61638738..61644562hg38UCSC Ensembl
chr16:61672845..61678250hg19UCSC Ensembl
Innerchr16:61672845..61678250hg19UCSC Ensembl
Outerchr16:61672642..61678466hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385406
hg195406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15496287
SamplesHG01060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638781
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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