A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507379



Internal ID20880669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68391953..68393028hg38UCSC Ensembl
chr16:68425856..68426931hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031701
Samples
Known GenesSMPD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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