A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042599



Internal ID21951915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10059..10059hg38UCSC Ensembl
chr1:10059..10059hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg383242
hg193242
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042599
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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