A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384468



Internal ID21042021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36203757..36205644hg38UCSC Ensembl
chr5:36203859..36205746hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg381888
hg191888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130441
Samples
Known GenesNADK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384468
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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