A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537382



Internal ID21861737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174076167..174076167hg38UCSC Ensembl
chr1:174045305..174045305hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041616
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537382
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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