A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170159



Internal ID21314220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:17488456..17502521hg38UCSC Ensembl
Outerchr3:17488053..17504946hg38UCSC Ensembl
Innerchr3:17529948..17544013hg19UCSC Ensembl
Outerchr3:17529545..17546438hg19UCSC Ensembl
Innerchr3:17504952..17519017hg18UCSC Ensembl
Outerchr3:17504549..17521442hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3816894
hg1916894
hg1816894
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242444, nssv14247927, nssv14243320
SamplesNGO_50, NGO_35, NGO_30
Known GenesTBC1D5
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170159
Frequency
Sample Size93
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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