A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935341



Internal ID21355410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173735920..173735920hg38UCSC Ensembl
chr5:173162923..173162923hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201610
SamplesHG002
Known GenesLOC101928136
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935341
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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