A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106107



Internal ID20673147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9216480..9220011hg38UCSC Ensembl
chr3:9258164..9261695hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg383532
hg193532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367644
Supporting Variants
Samples
Known GenesSRGAP3, SRGAP3-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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