A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922244



Internal ID22697469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137883676..137883742hg38UCSC Ensembl
chr7:137568422..137568488hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442633
Samples
Known GenesCREB3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922244
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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