A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389406



Internal ID22447276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71976309..71981751hg38UCSC Ensembl
chr17:69972450..69977892hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg385443
hg195443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936640
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389406
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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