A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913546



Internal ID22688762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130734621..130734691hg38UCSC Ensembl
chr7:130419382..130419452hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444510
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913546
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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