A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511988



Internal ID20885318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14264726..14274591hg38UCSC Ensembl
chr16:14358583..14368448hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg389866
hg199866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028450
Samples
Known GenesMKL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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