A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172340



Internal ID20739380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105188383..105240486hg38UCSC Ensembl
chr9:107950664..108002767hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3852104
hg1952104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452718
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172340
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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