A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626327



Internal ID21574632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132998904..132998904hg38UCSC Ensembl
chr5:132334596..132334596hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127547
SamplesNA19239
Known GenesZCCHC10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626327
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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