A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397671



Internal ID22455541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158710177..158713843hg38UCSC Ensembl
chr2:159566689..159570355hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg383667
hg193667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397671
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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