A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491631



Internal ID21149184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67449890..67456669hg38UCSC Ensembl
chr14:67916607..67923386hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg386780
hg196780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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