A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503216



Internal ID22561157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97779108..97782288hg38UCSC Ensembl
chr6:98226984..98230164hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg383181
hg193181
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5846501
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503216
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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