A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355156



Internal ID22580825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26396249..26397511hg38UCSC Ensembl
chr1:26722740..26724002hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381263
hg191263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355156
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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