A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249519



Internal ID21307114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87237542..87353136hg38UCSC Ensembl
Outerchr10:87216840..87357543hg38UCSC Ensembl
Innerchr10:88997299..89112893hg19UCSC Ensembl
Outerchr10:88976597..89117300hg19UCSC Ensembl
Innerchr10:88987279..89102873hg18UCSC Ensembl
Outerchr10:88966577..89107280hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38140704
hg19140704
hg18140704
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170175
Supporting Variants
SamplesNGO_32
Known GenesLOC439994, NUTM2A, NUTM2A-AS1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249519
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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