A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450365



Internal ID22508235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10358472..10359721hg38UCSC Ensembl
chr1:10418530..10419779hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5827569
Supporting Variants
Samples
Known GenesKIF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450365
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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