A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360096



Internal ID22585765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28874977..28879422hg38UCSC Ensembl
chr1:29201489..29205934hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg384446
hg194446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360096
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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