A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582291



Internal ID21530802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6078005..6078062hg38UCSC Ensembl
chr1:6138065..6138122hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065689
SamplesHG03486
Known GenesKCNAB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582291
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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