A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469229



Internal ID22527120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100572365..100574164hg38UCSC Ensembl
chr1:101037921..101039720hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5827662
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469229
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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