A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638901



Internal ID7025686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68024016..68030339hg38UCSC Ensembl
Innerchr16:68024045..68030311hg38UCSC Ensembl
Outerchr16:68023988..68030368hg38UCSC Ensembl
chr16:68057919..68064242hg19UCSC Ensembl
Innerchr16:68057948..68064214hg19UCSC Ensembl
Outerchr16:68057891..68064271hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg386324
hg196324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15501614, essv15501616, essv15501613, essv15501615
SamplesHG04214, HG01852, HG03863, HG00437
Known GenesDUS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638901
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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