A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094553



Internal ID20661593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119435910..119441068hg38UCSC Ensembl
chr3:119154757..119159915hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg385159
hg195159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361270
Supporting Variants
Samples
Known GenesTMEM39A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094553
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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