A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323153



Internal ID20856269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11665241..11666415hg38UCSC Ensembl
chr1:11725298..11726472hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381175
hg191175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051820
Samples
Known GenesFBXO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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