A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268790



Internal ID20478008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154951498..154951498hg38UCSC Ensembl
chr6:155272632..155272632hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268790
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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