A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408476



Internal ID21066029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115531270..115531650hg38UCSC Ensembl
chr5:114866967..114867347hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125628
Samples
Known GenesFEM1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408476
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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