A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170179



Internal ID21314240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16950828..16981517hg38UCSC Ensembl
Outerchr10:16948938..16982960hg38UCSC Ensembl
Innerchr10:16992827..17023516hg19UCSC Ensembl
Outerchr10:16990937..17024959hg19UCSC Ensembl
Innerchr10:17032833..17063522hg18UCSC Ensembl
Outerchr10:17030943..17064965hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3834023
hg1934023
hg1834023
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248808
SamplesNGO_32
Known GenesCUBN
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170179
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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