A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053536



Internal ID21962769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150781874..150781874hg38UCSC Ensembl
chr1:150754350..150754350hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053536
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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