A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096334



Internal ID20663375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149779406..149782288hg38UCSC Ensembl
chr3:149497193..149500075hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382883
hg192883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370342
Supporting Variants
Samples
Known GenesANKUB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096334
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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