A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384963



Internal ID22442833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45584205..45602251hg38UCSC Ensembl
chr1:46049877..46067923hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg3818047
hg1918047
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875892
Supporting Variants
Samples
Known GenesNASP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384963
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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