A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575522



Internal ID21523951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97716272..97716592hg38UCSC Ensembl
chr3:97435116..97435436hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126580
SamplesHG03125
Known GenesEPHA6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575522
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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