A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023378



Internal ID21932721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59509841..59513497hg38UCSC Ensembl
chr17:57587202..57590858hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg383657
hg193657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023378
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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