A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18118361



Internal ID20685401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55400590..55402823hg38UCSC Ensembl
chr4:56266757..56268990hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg382234
hg192234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385429
Supporting Variants
Samples
Known GenesTMEM165
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18118361
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02297


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