A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704693



Internal ID21376969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209681474..209683407hg38UCSC Ensembl
chr1:209854819..209856752hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381934
hg191934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389408
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704693
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0258621


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