A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945412



Internal ID21365481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136893196..136893196hg38UCSC Ensembl
chr3:136612038..136612038hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15189887
SamplesHG002
Known GenesNCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945412
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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