A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510037



Internal ID20883351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52369659..52511366hg38UCSC Ensembl
chr15:52661856..52803563hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38141708
hg19141708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024064
Samples
Known GenesMYO5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510037
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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