A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100814



Internal ID20667854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38220470..38221103hg38UCSC Ensembl
chr3:38261961..38262594hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370483
Supporting Variants
Samples
Known GenesOXSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100814
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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