A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705305



Internal ID21377581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241197238..241197552hg38UCSC Ensembl
chr1:241360538..241360852hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389523
Supporting Variants
Samples
Known GenesRGS7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705305
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.844828


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