A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403919



Internal ID21061472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115174711..115178125hg38UCSC Ensembl
chr5:114510408..114513822hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg383415
hg193415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122841
Samples
Known GenesTRIM36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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