A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083956



Internal ID21993189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37525736..37525736hg38UCSC Ensembl
chr17:35885839..35885839hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635373
Samples
Known GenesSYNRG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083956
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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