A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126580



Internal ID21469362
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 StatusS
Merged Variantsnsv5575522
Supporting Variants
SamplesHG03125
Known GenesEPHA6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126580
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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