A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601505



Internal ID21793552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66420721..66420826hg38UCSC Ensembl
chr15:66713059..66713164hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032082
Supporting Variants
Samples
Known GenesMAP2K1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601505
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