A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449325



Internal ID21106878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87933678..87939166hg38UCSC Ensembl
chr10:89693435..89698923hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg385489
hg195489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984837
Samples
Known GenesPTEN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449325
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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