A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468888



Internal ID22526778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114020586..114026157hg38UCSC Ensembl
chr1:114563208..114568779hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg385572
hg195572
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5827814
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468888
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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