A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528825



Internal ID22398216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:53965980..53966068hg38UCSC Ensembl
chr10:55725740..55725828hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347600, nssv14347595, nssv14347601, nssv14347598, nssv14347597, nssv14347594, nssv14347593, nssv14347599, nssv14347596
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesPCDH15
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528825
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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