A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15439577



Internal ID4193806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28217616..28220413hg38UCSC Ensembl
Innerchr16:28217638..28220391hg38UCSC Ensembl
Outerchr16:28217594..28220435hg38UCSC Ensembl
chr16:28228937..28231734hg19UCSC Ensembl
Innerchr16:28228959..28231712hg19UCSC Ensembl
Outerchr16:28228915..28231756hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382798
hg192798
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638332
Supporting Variants
SamplesHG03781
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15439577
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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