A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127683



Internal ID21469002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8439559..8439559hg38UCSC Ensembl
chr3:8481245..8481245hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610148
Supporting Variants
SamplesHG03125
Known GenesLMCD1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127683
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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