A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148678



Internal ID21503696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168281529..168281626hg38UCSC Ensembl
chr6:168682209..168682306hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582238
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148678
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