A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17478267



Internal ID22536168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44365973..44370280hg38UCSC Ensembl
chr17:42443341..42447648hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg384308
hg194308
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872089
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17478267
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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