A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188284



Internal ID20755324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41782105..41786608hg38UCSC Ensembl
chr15:42074303..42078806hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384504
hg194504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500165
Supporting Variants
Samples
Known GenesMAPKBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188284
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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