A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446645



Internal ID22504515
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 StatusS
Merged Variantsnsv5924585
Supporting Variants
Samples
Known GenesAGBL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446645
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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