A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251362



Internal ID21303705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87216840..87353136hg38UCSC Ensembl
Outerchr10:87215763..87357543hg38UCSC Ensembl
Innerchr10:88976597..89112893hg19UCSC Ensembl
Outerchr10:88975520..89117300hg19UCSC Ensembl
Innerchr10:88966577..89102873hg18UCSC Ensembl
Outerchr10:88965500..89107280hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38141781
hg19141781
hg18141781
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170175
Supporting Variants
SamplesMLY_8
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)nssv14251362
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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