A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170175



Internal ID21314236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87216840..87357543hg38UCSC Ensembl
Outerchr10:87215763..87371433hg38UCSC Ensembl
Innerchr10:88976597..89117300hg19UCSC Ensembl
Outerchr10:88975520..89131190hg19UCSC Ensembl
Innerchr10:88966577..89107280hg18UCSC Ensembl
Outerchr10:88965500..89121170hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38155671
hg19155671
hg18155671
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248369, nssv14244294, nssv14247897, nssv14251362, nssv14249519, nssv14241644, nssv14251974, nssv14245975, nssv14246464, nssv14250052, nssv14250883
SamplesNGO_3, SNI_8, MLY_17, MLY_12, SNI_7, NGO_32, NGO_6, MLY_8, SNI_5, NGO_11, SNI_4
Known GenesLOC439994, NUTM2A, NUTM2A-AS1, NUTM2D
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170175
Frequency
Sample Size93
Observed Gain9
Observed Loss2
Observed Complex0
Frequencyn/a


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