A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368587



Internal ID22594256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:199398592..199398650hg38UCSC Ensembl
chr1:199367720..199367778hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368587
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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