A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638039



Internal ID6678137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15651960..15653841hg38UCSC Ensembl
Innerchr16:15651960..15653841hg38UCSC Ensembl
Outerchr16:15651743..15654066hg38UCSC Ensembl
chr16:15745817..15747698hg19UCSC Ensembl
Innerchr16:15745817..15747698hg19UCSC Ensembl
Outerchr16:15745600..15747923hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg381882
hg191882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15385637
SamplesNA18745
Known GenesNDE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638039
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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