A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511497



Internal ID22569449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130118479..130123983hg38UCSC Ensembl
chr9:132880758..132886262hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg385505
hg195505
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852769
Supporting Variants
Samples
Known GenesGPR107
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511497
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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