A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157997



Internal ID21450487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13273560..13273560hg38UCSC Ensembl
chr6:13273792..13273792hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639337
Supporting Variants
SamplesHG01505
Known GenesPHACTR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157997
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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