A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3931010



Internal ID21351079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13494662..13494662hg38UCSC Ensembl
chr18:13494661..13494661hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185539
SamplesHG002
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3931010
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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