A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251179



Internal ID21301942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133152479..133317271hg38UCSC Ensembl
Outerchr9:133143357..133320783hg38UCSC Ensembl
Innerchr9:136027866..136184106hg19UCSC Ensembl
Outerchr9:136018744..136187620hg19UCSC Ensembl
Innerchr9:135017687..135173927hg18UCSC Ensembl
Outerchr9:135008565..135177441hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38177427
hg19168877
hg18168877
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169897
Supporting Variants
SamplesMLY_11
Known GenesABO, GBGT1, OBP2B, RALGDS
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251179
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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