A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628765



Internal ID21577070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149786185..149786185hg38UCSC Ensembl
chr6:150107321..150107321hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143006
SamplesHG00731
Known GenesPCMT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628765
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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