A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640560



Internal ID21588865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149803478..149803478hg38UCSC Ensembl
chr6:150124614..150124614hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141633
SamplesHG00731
Known GenesPCMT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640560
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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