A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047338



Internal ID21956572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8773839..8773839hg38UCSC Ensembl
chr1:8833898..8833898hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382564
hg192564
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531810
Samples
Known GenesRERE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047338
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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