A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882287



Internal ID22657264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6025840..6025907hg38UCSC Ensembl
chr1:6085900..6085967hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386521
Samples
Known GenesKCNAB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882287
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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