A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384690



Internal ID22442560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65181027..65183288hg38UCSC Ensembl
chr15:65473365..65475626hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382262
hg192262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931453
Supporting Variants
Samples
Known GenesCLPX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384690
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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