A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15373020



Internal ID2188964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10338302..10352664hg38UCSC Ensembl
Innerchr16:10338302..10352664hg38UCSC Ensembl
Outerchr16:10337802..10353164hg38UCSC Ensembl
chr16:10432159..10446521hg19UCSC Ensembl
Innerchr16:10432159..10446521hg19UCSC Ensembl
Outerchr16:10431659..10447021hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3814363
hg1914363
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637897
Supporting Variants
SamplesHG01974
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15373020
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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