A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353900



Internal ID22579569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234662368..234663355hg38UCSC Ensembl
chr1:234798114..234799101hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873851
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353900
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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