A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936297



Internal ID21356366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7803433..7803433hg38UCSC Ensembl
chr1:7863493..7863493hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191565
SamplesHG002
Known GenesPER3
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936297
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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