A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045071



Internal ID21954341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34541466..34541466hg38UCSC Ensembl
chr1:35007067..35007067hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523911
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045071
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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