A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381277



Internal ID21038830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11826201..11827100hg38UCSC Ensembl
chr5:11826313..11827212hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122952
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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