A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144967



Internal ID344172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38578874..38585000hg38UCSC Ensembl
chr15:38871075..38877201hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg386127
hg196127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701547
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144967
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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