A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458960



Internal ID22516842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25374215..25381253hg38UCSC Ensembl
chr1:25700706..25707744hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg387039
hg197039
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829658
Supporting Variants
Samples
Known GenesRHCE
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458960
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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