A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195033



Internal ID20762073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65517901..65538400hg38UCSC Ensembl
chr9:44794626..44815059hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3820500
hg1920434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447678
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.18992


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