A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194895



Internal ID20761935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25026969..25062443hg38UCSC Ensembl
chr9:25026967..25062441hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3835475
hg1935475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416000
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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