A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569899



Internal ID21761942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71375099..71375099hg38UCSC Ensembl
chr6:72084802..72084802hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076579
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569899
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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