A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459706



Internal ID22517592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32110113..32115962hg38UCSC Ensembl
chr1:32575714..32581563hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg385850
hg195850
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829989
Supporting Variants
Samples
Known GenesKPNA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459706
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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