A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130312



Internal ID21473358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8291713..8291787hg38UCSC Ensembl
chr3:8333400..8333474hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568476
Supporting Variants
SamplesHG03371
Known GenesLMCD1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130312
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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