A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076930



Internal ID21986163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94130650..94130650hg38UCSC Ensembl
chr5:93466355..93466355hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548970
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076930
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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