A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437220



Internal ID22495090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122337556..122341182hg38UCSC Ensembl
chr7:121977610..121981236hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg383627
hg193627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908707
Supporting Variants
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437220
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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