A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562986



Internal ID22431728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157523675..157523675hg38UCSC Ensembl
chr3:157241464..157241464hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14309052, nssv14309053, nssv14309047, nssv14309049, nssv14309051, nssv14309050, nssv14309048
SamplesHG00512, NA19238, HG00731, HG00732, NA19240, HG00733, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562986
Frequency
Sample Size9
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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