A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564325



Internal ID22433056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157213166..157213166hg38UCSC Ensembl
chr6:157534300..157534300hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14329704, nssv14329698, nssv14329705, nssv14329702, nssv14329697, nssv14329699, nssv14329700, nssv14329701, nssv14329703
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564325
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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