A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897288



Internal ID22672389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139849517..139849675hg38UCSC Ensembl
chr5:139229102..139229260hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416450
Samples
Known GenesNRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897288
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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