A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605993



Internal ID21798040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1508924..1508924hg38UCSC Ensembl
chr12:1618090..1618090hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085655
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605993
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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