A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504609



Internal ID20877871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105740005..105766379hg38UCSC Ensembl
chr14:106206342..106232716hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3826375
hg1926375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2294n223
Supporting Variantsnssv18016004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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