A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521969



Internal ID298244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3293873..3298973hg38UCSC Ensembl
chr16:3343873..3348973hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706352
Samples
Known GenesTIGD7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521969
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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