A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150673



Internal ID21503328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80485143..80485462hg38UCSC Ensembl
chr6:81194860..81195179hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571462
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150673
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