A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561211



Internal ID22429992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35022666..35022666hg38UCSC Ensembl
chr19:35513570..35513570hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286381
SamplesNA19239
Known GenesGRAMD1A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561211
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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