A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415230



Internal ID22473100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121139876..121140100hg38UCSC Ensembl
chr4:122061031..122061255hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903145
Supporting Variants
Samples
Known GenesTNIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415230
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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