A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365397



Internal ID22591066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159952544..159964327hg38UCSC Ensembl
chr1:159922334..159934117hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3811784
hg1911784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875026
Supporting Variants
Samples
Known GenesLINC01133, SLAMF9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365397
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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