A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575704



Internal ID21767747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14005782..14005782hg38UCSC Ensembl
chr6:14006013..14006013hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068045
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575704
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