A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746891



Internal ID20522907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57649248..57649462hg38UCSC Ensembl
chr17:55726609..55726823hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265049
Samples
Known GenesMSI2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746891
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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