A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15372776



Internal ID2800883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9299850..9301350hg38UCSC Ensembl
Innerchr16:9299873..9301327hg38UCSC Ensembl
Outerchr16:9299827..9301373hg38UCSC Ensembl
chr16:9393707..9395207hg19UCSC Ensembl
Innerchr16:9393730..9395184hg19UCSC Ensembl
Outerchr16:9393684..9395230hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381501
hg191501
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637871
Supporting Variants
SamplesHG02476
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15372776
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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