A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447553



Internal ID21105106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48347914..48353415hg38UCSC Ensembl
chr10:49555957..49561458hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg385502
hg195502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979979
Samples
Known GenesMAPK8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447553
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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