A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245975



Internal ID21313246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87310039..87353136hg38UCSC Ensembl
Outerchr10:87286741..87357543hg38UCSC Ensembl
Innerchr10:89069796..89112893hg19UCSC Ensembl
Outerchr10:89046498..89117300hg19UCSC Ensembl
Innerchr10:89059776..89102873hg18UCSC Ensembl
Outerchr10:89036478..89107280hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3870803
hg1970803
hg1870803
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170175
Supporting Variants
SamplesSNI_8
Known GenesLOC439994, NUTM2A-AS1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245975
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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