A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145732



Internal ID344937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1530694..1530745hg38UCSC Ensembl
chr16:1580695..1580746hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706694
Samples
Known GenesIFT140, TMEM204
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145732
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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