A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902865



Internal ID22678027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78392021..78392070hg38UCSC Ensembl
chr5:77687845..77687894hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416349
Samples
Known GenesSCAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902865
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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