A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707567



Internal ID21229362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165839973..165839973hg38UCSC Ensembl
chr6:166253461..166253461hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813573
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707567
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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