A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537744



Internal ID21862099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86138985..86138985hg38UCSC Ensembl
chr4:87060138..87060138hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075827
Supporting Variants
Samples
Known GenesMAPK10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537744
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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