A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930794



Internal ID21279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9196972..9198818hg38UCSC Ensembl
chr3:9238656..9240502hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381847
hg191847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441454
Supporting Variants
Samples
Known GenesSRGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930794
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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