A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140877



Internal ID21456830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93040131..93040131hg38UCSC Ensembl
chr6:93749849..93749849hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg388007
hg198007
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627625
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140877
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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