A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392149



Internal ID21049702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35072861..35077266hg38UCSC Ensembl
chr5:35072963..35077368hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg384406
hg194406
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213402
Samples
Known GenesPRLR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392149
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