A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015919



Internal ID20582959
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 StatusS
Merged Variantsnsv6503983
Supporting Variants
Samples
Known GenesMARK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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