A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151693



Internal ID21405281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131482153..131482255hg38UCSC Ensembl
chr6:131803293..131803395hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575039
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151693
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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