A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15385637



Internal ID5387453
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638039
Supporting Variants
SamplesNA18745
Known GenesNDE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15385637
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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