A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094107



Internal ID20661147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127628301..127629600hg38UCSC Ensembl
chr3:127347144..127348443hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372660
Supporting Variants
Samples
Known GenesPODXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.06069


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