A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510896



Internal ID20884219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103462009..103466935hg38UCSC Ensembl
chr14:103928346..103933272hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg384927
hg194927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015917
Samples
Known GenesMARK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510896
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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