A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323282



Internal ID20856399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15507190..15514366hg38UCSC Ensembl
chr1:15833685..15840861hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg387177
hg197177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052055
Samples
Known GenesCASP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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