A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509227



Internal ID20882535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52465003..52475089hg38UCSC Ensembl
chr15:52757200..52767286hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3810087
hg1910087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024071
Samples
Known GenesMYO5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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