A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604147



Internal ID20977218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158998012..158999210hg38UCSC Ensembl
chr6:159419044..159420242hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216713
Samples
Known GenesRSPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604147
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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