A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561430



Internal ID21885785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90369341..90369341hg38UCSC Ensembl
chr6:91079060..91079060hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6078048
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561430
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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