A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445131



Internal ID22503001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86321136..86321511hg38UCSC Ensembl
chr9:88936051..88936426hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925537
Supporting Variants
Samples
Known GenesZCCHC6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445131
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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