A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498138



Internal ID20871346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23588206..23588729hg38UCSC Ensembl
chr16:23599527..23600050hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028799
Samples
Known GenesNDUFAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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