A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881241



Internal ID22656215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10274673..10274758hg38UCSC Ensembl
chr1:10334731..10334816hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362251
Samples
Known GenesKIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881241
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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