A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573928



Internal ID21765971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139468772..139468772hg38UCSC Ensembl
chr6:139789909..139789909hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573928
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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