A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575949



Internal ID21767992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93143462..93143462hg38UCSC Ensembl
chr6:93853180..93853180hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079802
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575949
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer