A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030952



Internal ID21940295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52206316..52206398hg38UCSC Ensembl
chr15:52498513..52498595hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603063
Samples
Known GenesMYO5C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030952
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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