A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510585



Internal ID20883905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52462733..52468597hg38UCSC Ensembl
chr15:52754930..52760794hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg385865
hg195865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024070
Samples
Known GenesMYO5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510585
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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