A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388366



Internal ID22446236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31974558..31975128hg38UCSC Ensembl
chr1:32440159..32440729hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868410
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388366
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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