A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046805



Internal ID21956038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23837086..23837086hg38UCSC Ensembl
chr1:24163576..24163576hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046805
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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