A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370173



Internal ID22595842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43011303..43012388hg38UCSC Ensembl
chr17:41163320..41164405hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932664
Supporting Variants
Samples
Known GenesIFI35
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370173
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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