A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145318



Internal ID344523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82322874..82328874hg38UCSC Ensembl
chr15:82615210..82621230hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386001
hg196021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704058
Samples
Known GenesADAMTS7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145318
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer