A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607335



Internal ID21799382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45236941..45236941hg38UCSC Ensembl
chr14:45706144..45706144hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080480
Supporting Variants
Samples
Known GenesMIS18BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607335
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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