A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145432



Internal ID344637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29896874..29902200hg38UCSC Ensembl
chr19:30387781..30393107hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg385327
hg195327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145432
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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