A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028856



Internal ID21938199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31659170..31659251hg38UCSC Ensembl
chr17:29986189..29986270hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622577
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028856
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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