A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021963



Internal ID21931306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76916128..76916223hg38UCSC Ensembl
chr17:74912210..74912305hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633669
Samples
Known GenesMGAT5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021963
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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