A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510855



Internal ID22568806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113102599..113132758hg38UCSC Ensembl
chr9:115864879..115895038hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3830160
hg1930160
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851379
Supporting Variants
Samples
Known GenesFAM225A, FAM225B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510855
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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