A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434989



Internal ID22492859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76506341..76509728hg38UCSC Ensembl
chr9:79121257..79124644hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383388
hg193388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924630
Supporting Variants
Samples
Known GenesGCNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434989
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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