A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558475



Internal ID21882830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134449363..134449363hg38UCSC Ensembl
chr6:134770501..134770501hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6077006
Supporting Variants
Samples
Known GenesLINC01010
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558475
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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