A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564474



Internal ID22433204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70409646..70409646hg38UCSC Ensembl
chr6:71119349..71119349hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14329245, nssv14329246, nssv14329244, nssv14329247, nssv14329243
SamplesNA19239, HG00731, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564474
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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