A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400349



Internal ID21057902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46159779..46160259hg38UCSC Ensembl
chr6:46127516..46127996hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144210
Samples
Known GenesENPP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400349
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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