A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528756



Internal ID22398147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60468973..60469347hg38UCSC Ensembl
chr10:62228731..62229105hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349550, nssv14349551
SamplesNA19238, HG00731
Known GenesANK3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528756
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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