A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441788



Internal ID21099341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48333801..48336500hg38UCSC Ensembl
chr10:49541844..49544543hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979977
Samples
Known GenesMAPK8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441788
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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