A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176767



Internal ID20743808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126757587..126767662hg38UCSC Ensembl
chr9:129519866..129529941hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3810076
hg1910076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437572
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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