A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3544644



Internal ID22413677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36107429..36107429hg38UCSC Ensembl
chr14:36576635..36576635hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14444999
SamplesHG00733
Known GenesLINC00609
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3544644
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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