A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079808



Internal ID21405852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67835542..67835542hg38UCSC Ensembl
chr12:68229322..68229322hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649608
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079808
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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