A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451490



Internal ID22509362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12220352..12222879hg38UCSC Ensembl
chr1:12280409..12282936hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382528
hg192528
Variant TypeOTHER copy number variation
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5827949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451490
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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