A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651602



Internal ID21599907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56881031..56881031hg38UCSC Ensembl
chr17:54958392..54958392hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093689
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651602
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