A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484198



Internal ID21141751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62246595..62395140hg38UCSC Ensembl
chr14:62713313..62861858hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38148546
hg19148546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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