A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512280



Internal ID20885612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52018101..52020200hg38UCSC Ensembl
chr15:52310298..52312397hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183996
Samples
Known GenesMAPK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512280
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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