A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217123



Internal ID20784163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151492501..151496600hg38UCSC Ensembl
chr6:151813636..151817735hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606378
Supporting Variants
Samples
Known GenesCCDC170
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217123
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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