A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373424



Internal ID22599093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:79994486..79994660hg38UCSC Ensembl
chr1:80460171..80460345hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869760
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373424
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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