A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924585



Internal ID22699812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135096480..135096662hg38UCSC Ensembl
chr7:134781232..134781414hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446645
Samples
Known GenesAGBL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924585
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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