A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059912



Internal ID21431932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110310153..110310153hg38UCSC Ensembl
chr1:110852775..110852775hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611279
Supporting Variants
SamplesHG00731
Known GenesLOC440600
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059912
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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