A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045647



Internal ID21954911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78240927..78240927hg38UCSC Ensembl
chr1:78706611..78706611hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529531
Samples
Known GenesMGC27382
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045647
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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