A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083856



Internal ID21438893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4119916..4119916hg38UCSC Ensembl
chr12:4229082..4229082hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656766
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083856
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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