A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637904



Internal ID7024692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10504113..10523959hg38UCSC Ensembl
Innerchr16:10504113..10523959hg38UCSC Ensembl
Outerchr16:10503613..10524459hg38UCSC Ensembl
chr16:10597970..10617816hg19UCSC Ensembl
Innerchr16:10597970..10617816hg19UCSC Ensembl
Outerchr16:10597470..10618316hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3819847
hg1919847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15373029
SamplesHG01260
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637904
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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