A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042536



Internal ID21951852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10001..10001hg38UCSC Ensembl
chr1:249240600..249240600hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg382663
hg192663
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042536
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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