A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387261



Internal ID21044814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18966286..19604176hg38UCSC Ensembl
chr5:18966395..19604285hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38637891
hg19637891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127449
Samples
Known GenesCDH18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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