A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368191



Internal ID22593860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160691932..160699963hg38UCSC Ensembl
chr1:160661722..160669753hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg388032
hg198032
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876749
Supporting Variants
Samples
Known GenesCD48
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368191
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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