A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414675



Internal ID22472545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159906702..159910486hg38UCSC Ensembl
chr6:160327734..160331518hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383785
hg193785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906619
Supporting Variants
Samples
Known GenesMAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414675
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