A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496893



Internal ID20870096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52328467..52413255hg38UCSC Ensembl
chr15:52620664..52705452hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3884789
hg1984789
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182274
Samples
Known GenesMYO5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496893
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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