A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388359



Internal ID22446229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31854708..31854817hg38UCSC Ensembl
chr17:30181727..30181836hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928077
Supporting Variants
Samples
Known GenesCOPRS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388359
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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