A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508867



Internal ID20882171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97663688..97674612hg38UCSC Ensembl
chr14:98130025..98140949hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810925
hg1910925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2240n223
Supporting Variantsnssv18022511
Samples
Known GenesLOC100129345
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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