A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392638



Internal ID22450508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95282021..95290980hg38UCSC Ensembl
chr1:95747577..95756536hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg388960
hg198960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882658
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392638
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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