A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145118



Internal ID344323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29825630..29826080hg38UCSC Ensembl
chr19:30316537..30316987hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145118
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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