A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399242



Internal ID21056795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152394338..152394781hg38UCSC Ensembl
chr5:151773899..151774342hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126996
Samples
Known GenesNMUR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399242
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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