A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923593



Internal ID22698820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129201247..129201880hg38UCSC Ensembl
chr7:128841088..128841721hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430961
Samples
Known GenesSMO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923593
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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