A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501633



Internal ID20874870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82199947..82501878hg38UCSC Ensembl
chr15:82492288..83170860hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38301932
hg19678573
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184965
Samples
Known GenesADAMTS7P1, CSPG4P8, EFTUD1, FAM154B, GOLGA6L10, GOLGA6L20, GOLGA6L9, LOC727751, LOC80154, RPS17, RPS17L, UBE2Q2P2, UBE2Q2P3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501633
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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