A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944944



Internal ID21365013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166997813..166997813hg38UCSC Ensembl
chr6:167411301..167411301hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381454
hg191454
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203248
SamplesHG002
Known GenesMIR3939
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944944
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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