A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595883



Internal ID21787926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36645311..36645311hg38UCSC Ensembl
chr9:36645308..36645308hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083157
Supporting Variants
Samples
Known GenesMELK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595883
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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