A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901063



Internal ID22676211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177336824..177336975hg38UCSC Ensembl
chr5:176763825..176763976hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415225
Samples
Known GenesLMAN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901063
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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