A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407800



Internal ID21065353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119216601..119217700hg38UCSC Ensembl
chr5:118552296..118553395hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125777
Samples
Known GenesDMXL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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