A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077127



Internal ID21986360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:105942385..105942385hg38UCSC Ensembl
chr5:105278086..105278086hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077127
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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