A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177731



Internal ID20744771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76838548..76849580hg38UCSC Ensembl
chr9:79453464..79464496hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3811033
hg1911033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453438
Supporting Variants
Samples
Known GenesPRUNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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