A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633006



Internal ID21581311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131996994..131996994hg38UCSC Ensembl
chr5:131332687..131332687hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128315
SamplesNA19238
Known GenesACSL6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633006
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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