A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606671



Internal ID21798718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36801908..36801908hg38UCSC Ensembl
chr15:37094109..37094109hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6098581
Supporting Variants
Samples
Known GenesC15orf41, CSNK1A1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606671
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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