A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572277



Internal ID21520664
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 StatusM
Merged Variants
Supporting Variantsnssv17132197
SamplesHG00512
Known GenesCLK4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572277
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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