A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892484



Internal ID22667535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91065250..91065301hg38UCSC Ensembl
chr5:90361067..90361118hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420853
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892484
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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