A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223470



Internal ID20790510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71869788..71922689hg38UCSC Ensembl
chr9:74484704..74537605hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3852902
hg1952902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447904
Supporting Variants
Samples
Known GenesABHD17B, C9orf85
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223470
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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