A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170074



Internal ID21314135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119373876..119483902hg38UCSC Ensembl
Outerchr10:119371707..119488704hg38UCSC Ensembl
Innerchr10:121133388..121243414hg19UCSC Ensembl
Outerchr10:121131219..121248216hg19UCSC Ensembl
Innerchr10:121123378..121233404hg18UCSC Ensembl
Outerchr10:121121209..121238206hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38116998
hg19116998
hg18116998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252383
SamplesNGO_25
Known GenesGRK5, MIR4681
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170074
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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