A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607370



Internal ID21555675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17431359..17431359hg38UCSC Ensembl
chr1:17757855..17757855hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061934
SamplesHG00732
Known GenesRCC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607370
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