A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509182



Internal ID20882489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52052636..52062737hg38UCSC Ensembl
chr15:52344833..52354934hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3810102
hg1910102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024050
Samples
Known GenesMAPK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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