A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636191



Internal ID21828238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33198201..33198201hg38UCSC Ensembl
chr17:31525219..31525219hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100091
Supporting Variants
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636191
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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