A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093865



Internal ID21465071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64969421..64969421hg38UCSC Ensembl
chr17:62965539..62965539hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664403
Supporting Variants
SamplesHG03065
Known GenesAMZ2P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093865
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