A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418091



Internal ID22475961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70525893..70526123hg38UCSC Ensembl
chr4:71391610..71391840hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901531
Supporting Variants
Samples
Known GenesAMTN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418091
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