A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144722



Internal ID343927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29057800..29070486hg38UCSC Ensembl
chr16:29069121..29081807hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3812687
hg1912687
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144722
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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