A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106105



Internal ID20673145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9205784..9207609hg38UCSC Ensembl
chr3:9247468..9249293hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381826
hg191826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359296
Supporting Variants
Samples
Known GenesSRGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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