A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250052



Internal ID21312892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87310987..87335259hg38UCSC Ensembl
Outerchr10:87310039..87335788hg38UCSC Ensembl
Innerchr10:89070744..89095016hg19UCSC Ensembl
Outerchr10:89069796..89095545hg19UCSC Ensembl
Innerchr10:89060724..89084996hg18UCSC Ensembl
Outerchr10:89059776..89085525hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3825750
hg1925750
hg1825750
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170175
Supporting Variants
SamplesSNI_5
Known GenesNUTM2A-AS1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250052
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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