A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17491571



Internal ID22549496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47261602..47263701hg38UCSC Ensembl
chr3:47303092..47305191hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836576
Supporting Variants
Samples
Known GenesKIF9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17491571
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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