A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025119



Internal ID21934462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50683383..50683500hg38UCSC Ensembl
chr18:48209753..48209870hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635159
Samples
Known GenesMAPK4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025119
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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