A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496932



Internal ID20870135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48904706..48912565hg38UCSC Ensembl
chr16:48938617..48946476hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg387860
hg197860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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