A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705338



Internal ID21377614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244731615..244736314hg38UCSC Ensembl
chr1:244894917..244899616hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389526
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705338
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0114943


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