A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747557



Internal ID20523576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84165777..84244697hg38UCSC Ensembl
chr15:84834529..84913449hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3878921
hg1978921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280833
Samples
Known GenesGOLGA6L4, LOC100505679, LOC388152, LOC440300, LOC642423
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747557
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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