A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094821



Internal ID22004054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30237151..30237151hg38UCSC Ensembl
chr17:28564169..28564169hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094821
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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