A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600738



Internal ID20973809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145814001..145816000hg38UCSC Ensembl
chr6:146135137..146137136hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216951
Samples
Known GenesFBXO30, LOC100507557
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600738
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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