A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063792



Internal ID21491427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240536567..240536668hg38UCSC Ensembl
chr1:240699867..240699968hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571809
Supporting Variants
SamplesNA19238
Known GenesGREM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063792
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