A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552250



Internal ID21876605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155343460..155409898hg38UCSC Ensembl
chr4:156264612..156331050hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3866439
hg1966439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995514
Supporting Variants
Samples
Known GenesMAP9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552250
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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