A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465740



Internal ID22523629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47161346..47167104hg38UCSC Ensembl
chr1:47627018..47632776hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg385759
hg195759
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830066
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465740
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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