A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425971



Internal ID22483841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55420107..55420107hg38UCSC Ensembl
chr4:56286274..56286274hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5958971
Supporting Variants
Samples
Known GenesTMEM165
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425971
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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