A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051678



Internal ID21960911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2825780..3839984hg38UCSC Ensembl
chr20:2806426..3820631hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381014205
hg191014206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620661
Samples
Known GenesADAM33, AP5S1, ATRN, AVP, C20orf194, C20orf27, CDC25B, CENPB, DDRGK1, FASTKD5, GFRA4, GNRH2, HSPA12B, ITPA, LZTS3, MRPS26, OXT, PCED1A, PTPRA, SIGLEC1, SLC4A11, SPEF1, UBOX5, UBOX5-AS1, VPS16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051678
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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