A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170050



Internal ID21314111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143576864..143593356hg38UCSC Ensembl
Outerchr3:143575340..143602848hg38UCSC Ensembl
Innerchr3:143295706..143312198hg19UCSC Ensembl
Outerchr3:143294182..143321690hg19UCSC Ensembl
Innerchr3:144778396..144794888hg18UCSC Ensembl
Outerchr3:144776872..144804380hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3827509
hg1927509
hg1827509
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242882
SamplesNGO_24
Known GenesSLC9A9
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170050
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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