A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454687



Internal ID22512563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125977330..125980179hg38UCSC Ensembl
chr10:127665899..127668748hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382850
hg192850
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855085
Supporting Variants
Samples
Known GenesFANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454687
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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