A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386846



Internal ID21044399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:22277916..22762976hg38UCSC Ensembl
chr5:22278025..22763085hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38485061
hg19485061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131056
Samples
Known GenesCDH12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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