A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606953



Internal ID21799000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67609444..67609503hg38UCSC Ensembl
chr15:67901782..67901841hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020875
Supporting Variants
Samples
Known GenesMAP2K5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606953
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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