A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15474635



Internal ID3696844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49254386..49255208hg38UCSC Ensembl
Innerchr16:49254389..49255205hg38UCSC Ensembl
Outerchr16:49254383..49255211hg38UCSC Ensembl
chr16:49288297..49289119hg19UCSC Ensembl
Innerchr16:49288300..49289116hg19UCSC Ensembl
Outerchr16:49288294..49289122hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38823
hg19823
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638591
Supporting Variants
SamplesHG03300
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15474635
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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