A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610801



Internal ID21559106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2080410..2080410hg38UCSC Ensembl
chr4:2082137..2082137hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132550, nssv17121254
SamplesHG00731, NA18939
Known GenesPOLN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610801
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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