A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371269



Internal ID22596938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59405393..59405490hg38UCSC Ensembl
chr17:57482754..57482851hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943193
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371269
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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