A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892737



Internal ID22667791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91323041..91421784hg38UCSC Ensembl
chr4:92244192..92342935hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3898744
hg1998744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416997
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892737
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