A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467858



Internal ID22525748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10013252..10016151hg38UCSC Ensembl
chr1:10073310..10076209hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5827870
Supporting Variants
Samples
Known GenesRBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467858
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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