A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499578



Internal ID20872799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67893001..67893700hg38UCSC Ensembl
chr16:67926904..67927603hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030842
Samples
Known GenesPSKH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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