A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534090



Internal ID21858446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50217061..50217061hg38UCSC Ensembl
chr1:50682733..50682733hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg386226
hg196226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059867
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534090
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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