A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372742



Internal ID22598411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43872135..43874494hg38UCSC Ensembl
chr17:41949503..41951862hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382360
hg192360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932932
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372742
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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