A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534372



Internal ID21858728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50592252..50592252hg38UCSC Ensembl
chr1:51057924..51057924hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6055858
Supporting Variants
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534372
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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