A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358819



Internal ID22584488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240393919..240394876hg38UCSC Ensembl
chr1:240557219..240558176hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38958
hg19958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873286
Supporting Variants
Samples
Known GenesFMN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358819
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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