A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442038



Internal ID21099591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87941675..87942370hg38UCSC Ensembl
chr10:89701432..89702127hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984840
Samples
Known GenesPTEN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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