A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638332



Internal ID7025118
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15439577, essv15439578
SamplesHG03781, HG03951
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638332
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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