A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435774



Internal ID22493644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76467302..76468156hg38UCSC Ensembl
chr9:79082218..79083072hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918369
Supporting Variants
Samples
Known GenesGCNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435774
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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