A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17447211



Internal ID22505081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:118056089..118062836hg38UCSC Ensembl
chr7:117696143..117702890hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg386748
hg196748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911918
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17447211
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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