A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169798



Internal ID21313609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126112035..126200187hg38UCSC Ensembl
Outerchr9:126108555..126203830hg38UCSC Ensembl
Innerchr9:128874314..128962466hg19UCSC Ensembl
Outerchr9:128870834..128966109hg19UCSC Ensembl
Innerchr9:127914135..128002287hg18UCSC Ensembl
Outerchr9:127910655..128005930hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3895276
hg1995276
hg1895276
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247254, nssv14242523
SamplesNGO_1, MLY_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169798
Frequency
Sample Size93
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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