A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576848



Internal ID21768891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165122252..165122252hg38UCSC Ensembl
chr6:165535741..165535741hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076505
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576848
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