A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410222



Internal ID22468092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3895853..4163425hg38UCSC Ensembl
chr4:3897580..4165152hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38267573
hg19267573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897384
Supporting Variants
Samples
Known GenesFAM86EP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410222
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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