A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405959



Internal ID21063512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2658578..2666528hg38UCSC Ensembl
chr6:2658812..2666762hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg387951
hg197951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140759
Samples
Known GenesMYLK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405959
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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