A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946369



Internal ID21366439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49701610..49701610hg38UCSC Ensembl
chr6:49669323..49669323hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15201988
SamplesHG002
Known GenesCRISP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946369
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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