A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143550



Internal ID21481142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143814595..143814595hg38UCSC Ensembl
chr6:144135732..144135732hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628915
Supporting Variants
SamplesHG03683
Known GenesPHACTR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143550
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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