A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132197



Internal ID21406316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178609627..178609852hg38UCSC Ensembl
chr5:178036628..178036853hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572277
Supporting Variants
SamplesHG00512
Known GenesCLK4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132197
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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