A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664155



Internal ID21612460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3600715..3600715hg38UCSC Ensembl
chr18:3600713..3600713hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100882
SamplesHG00732
Known GenesDLGAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664155
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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