A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094079



Internal ID21492205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64581798..64581798hg38UCSC Ensembl
chr12:64975578..64975578hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658471
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094079
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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