A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706860



Internal ID21379136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50303776..50305719hg38UCSC Ensembl
chr1:50769448..50771391hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381944
hg191944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390979
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706860
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00574713


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