A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425885



Internal ID22483755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55401114..55401114hg38UCSC Ensembl
chr4:56267281..56267281hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967210
Supporting Variants
Samples
Known GenesTMEM165
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425885
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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