A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528844



Internal ID21853201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37629486..37629486hg38UCSC Ensembl
chr1:38095158..38095158hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382361
hg192361
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052653
Supporting Variants
Samples
Known GenesRSPO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528844
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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