A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440566



Internal ID21098119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94088127..94090387hg38UCSC Ensembl
chr10:95847884..95850144hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg382261
hg192261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985237
Samples
Known GenesPLCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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