A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573714



Internal ID21765757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140059519..140064451hg38UCSC Ensembl
chr6:140380656..140385588hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg384933
hg194933
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004333
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573714
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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