A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388365



Internal ID22446235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7913111..7913456hg38UCSC Ensembl
chr1:7973171..7973516hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870227
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388365
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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