A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15354686



Internal ID5356502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:146435..159074hg38UCSC Ensembl
Innerchr16:146498..159012hg38UCSC Ensembl
Outerchr16:146373..159137hg38UCSC Ensembl
chr16:196434..209073hg19UCSC Ensembl
Innerchr16:196497..209011hg19UCSC Ensembl
Outerchr16:196372..209136hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3812640
hg1912640
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637543
Supporting Variants
SamplesHG01855
Known GenesHBZ
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15354686
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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