A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176675



Internal ID20743716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125264785..125265489hg38UCSC Ensembl
chr9:128027064..128027768hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453072
Supporting Variants
Samples
Known GenesGAPVD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00096


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