A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511494



Internal ID22569446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130110645..130116628hg38UCSC Ensembl
chr9:132872924..132878907hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg385984
hg195984
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860384
Supporting Variants
Samples
Known GenesGPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511494
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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