A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390344



Internal ID21047897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:12397418..12921682hg38UCSC Ensembl
chr5:12397530..12921794hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38524265
hg19524265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5642n223
Supporting Variantsnssv18124503
Samples
Known GenesCT49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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