A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202939



Internal ID21341745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165749182..165749182hg38UCSC Ensembl
chr6:166162670..166162670hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3932552
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202939
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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