A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512416



Internal ID20885750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102296927..102300110hg38UCSC Ensembl
chr14:102763264..102766447hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg383184
hg193184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015646
Samples
Known GenesMOK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512416
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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