A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497602



Internal ID22555536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105274928..105276020hg38UCSC Ensembl
chr4:106196085..106197177hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381093
hg191093
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836952
Supporting Variants
Samples
Known GenesTET2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497602
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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