A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247254



Internal ID21304020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126182006..126192030hg38UCSC Ensembl
Outerchr9:126176512..126192290hg38UCSC Ensembl
Innerchr9:128944285..128954309hg19UCSC Ensembl
Outerchr9:128938791..128954569hg19UCSC Ensembl
Innerchr9:127984106..127994130hg18UCSC Ensembl
Outerchr9:127978612..127994390hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3815779
hg1915779
hg1815779
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169798
Supporting Variants
SamplesNGO_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247254
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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