A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503983



Internal ID20877241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103485087..103486157hg38UCSC Ensembl
chr14:103951424..103952494hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381071
hg191071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015919
Samples
Known GenesMARK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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