A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499699



Internal ID22557635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152662363..152693181hg38UCSC Ensembl
chr4:153583515..153614333hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3830819
hg1930819
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5838066
Supporting Variants
Samples
Known GenesTMEM154
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499699
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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