A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417968



Internal ID22475838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20433993..20437260hg38UCSC Ensembl
chr4:20435616..20438883hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg383268
hg193268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897783
Supporting Variants
Samples
Known GenesSLIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417968
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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