A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413195



Internal ID22471065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103597249..103605409hg38UCSC Ensembl
chr4:104518406..104526566hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg388161
hg198161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893984
Supporting Variants
Samples
Known GenesTACR3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413195
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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