A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145403



Internal ID344608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34161700..34176700hg38UCSC Ensembl
chr16:33964167..33979167hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3815001
hg1915001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145403
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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