A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111102



Internal ID20678142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158223675..158224198hg38UCSC Ensembl
chr4:159144827..159145350hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388526
Supporting Variants
Samples
Known GenesTMEM144
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111102
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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