A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127798



Internal ID21405960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8382817..8382817hg38UCSC Ensembl
chr3:8424503..8424503hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615481
Supporting Variants
SamplesHG00512
Known GenesLMCD1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127798
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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