A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145679



Internal ID344884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13790000..13806000hg38UCSC Ensembl
chr19:13900814..13916814hg19UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg3816001
hg1916001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721626
Samples
Known GenesZSWIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145679
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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