A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434652



Internal ID22492522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55056368..55056368hg38UCSC Ensembl
chr6:54921166..54921166hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961702
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434652
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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