A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937118



Internal ID21357187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2145621..2145621hg38UCSC Ensembl
chr5:2145735..2145735hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200954
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937118
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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