A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400333



Internal ID21057886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138071509..138086942hg38UCSC Ensembl
chr5:137407198..137422631hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3815434
hg1915434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125318
Samples
Known GenesWNT8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400333
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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