A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264074



Internal ID20831114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9218881..9219749hg38UCSC Ensembl
chr3:9260565..9261433hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38869
hg19869
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554724
Supporting Variants
Samples
Known GenesSRGAP3, SRGAP3-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264074
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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