A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155719



Internal ID21425767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36429253..36429253hg38UCSC Ensembl
chr6:36397030..36397030hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628438
Supporting Variants
SamplesHG00731
Known GenesPXT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155719
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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