A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462207



Internal ID22520092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26211699..26213530hg38UCSC Ensembl
chr1:26538190..26540021hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381832
hg191832
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829929
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462207
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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