A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932191



Internal ID21352260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176591689..176591689hg38UCSC Ensembl
chr5:176018690..176018690hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201846
SamplesHG002
Known GenesCDHR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932191
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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