A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079679



Internal ID21490036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6227195..6227195hg38UCSC Ensembl
chr12:6336361..6336361hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651337
Supporting Variants
SamplesNA19238
Known GenesCD9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079679
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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