A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606605



Internal ID21798652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55420649..55438648hg38UCSC Ensembl
chr15:55712847..55730846hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3818000
hg1918000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029048
Supporting Variants
Samples
Known GenesDYX1C1, DYX1C1-CCPG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606605
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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