A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145630



Internal ID344835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29379954..29380284hg38UCSC Ensembl
chr16:29391275..29391605hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145630
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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