A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511648



Internal ID22569600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133179427..133187200hg38UCSC Ensembl
chr9:136054814..136062587hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg387774
hg197774
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847627
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511648
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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