A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526181



Internal ID21850539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30744289..30744289hg38UCSC Ensembl
chr1:31217136..31217136hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043678
Supporting Variants
Samples
Known GenesLAPTM5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526181
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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