A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573601



Internal ID21522007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8668894..8668993hg38UCSC Ensembl
chr1:8728953..8729052hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067047
SamplesHG00731
Known GenesRERE
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573601
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