A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643296



Internal ID21591601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138572247..138572247hg38UCSC Ensembl
chr5:137907936..137907936hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg382727
hg192727
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135334
SamplesNA19239
Known GenesHSPA9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643296
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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