A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572730



Internal ID21521123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65732256..65734552hg38UCSC Ensembl
chr5:65028083..65030379hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg382297
hg192297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155305
SamplesHG00732
Known GenesNLN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572730
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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