A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482202



Internal ID21139755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56319068..56319409hg38UCSC Ensembl
chr14:56785786..56786127hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482202
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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