A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191236



Internal ID20758276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7300201..7387100hg38UCSC Ensembl
chr9:7300201..7387100hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3886900
hg1986900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424050
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191236
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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