A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381816



Internal ID22439686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17632331..17632535hg38UCSC Ensembl
chr17:17535645..17535849hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381816
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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