A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604942



Internal ID20978013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130343755..130358810hg38UCSC Ensembl
chr6:130664900..130679955hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg3815056
hg1915056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138454
Samples
Known GenesSAMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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