A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703772



Internal ID21376048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42425034..42426716hg38UCSC Ensembl
chr6:42392772..42394454hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381683
hg191683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392352
Supporting Variants
Samples
Known GenesTRERF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703772
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00574713


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