A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362238



Internal ID21019791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188146421..188284686hg38UCSC Ensembl
chr3:187864209..188002474hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38138266
hg19138266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212232
Samples
Known GenesFLJ42393, LPP, LPP-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362238
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