A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829553



Internal ID22604488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235621919..235627627hg38UCSC Ensembl
chr1:235785219..235790927hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg385709
hg195709
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463011
Samples
Known GenesGNG4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829553
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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