A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573940



Internal ID21765983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119289432..119289534hg38UCSC Ensembl
chr6:119610597..119610699hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000653
Supporting Variants
Samples
Known GenesMAN1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573940
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