A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098746



Internal ID22007979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38594634..38594634hg38UCSC Ensembl
chr17:36750887..36750887hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626328
Samples
Known GenesSRCIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098746
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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