A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656186



Internal ID21604491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13494662..13494662hg38UCSC Ensembl
chr18:13494661..13494661hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100495
SamplesHG00731
Known GenesLDLRAD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656186
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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