A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404664



Internal ID22462534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9111498..9112087hg38UCSC Ensembl
chr18:9111496..9112085hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940682
Supporting Variants
Samples
Known GenesNDUFV2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404664
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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