A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15373036



Internal ID1580953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10632967..10636172hg38UCSC Ensembl
Innerchr16:10632967..10636172hg38UCSC Ensembl
Outerchr16:10632857..10636298hg38UCSC Ensembl
chr16:10726824..10730029hg19UCSC Ensembl
Innerchr16:10726824..10730029hg19UCSC Ensembl
Outerchr16:10726714..10730155hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg383206
hg193206
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637909
Supporting Variants
SamplesHG01462
Known GenesTEKT5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15373036
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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