A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357070



Internal ID22582739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110396018..110396095hg38UCSC Ensembl
chr1:110938640..110938717hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357070
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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