A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383861



Internal ID21041414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16909478..16911993hg38UCSC Ensembl
chr5:16909587..16912102hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382516
hg192516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129552
Samples
Known GenesMYO10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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