A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736718



Internal ID20512670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:19915308..21012170hg38UCSC Ensembl
chr15:20120561..21217499hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381096863
hg191096939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279698
Samples
Known GenesCHEK2P2, CT60, GOLGA6L6, GOLGA8CP, HERC2P3, NBEAP1, NF1P2, POTEB, POTEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736718
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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