A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568562



Internal ID21516911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6025840..6025924hg38UCSC Ensembl
chr1:6085900..6085984hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067202
SamplesNA12329
Known GenesKCNAB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568562
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