A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045020



Internal ID19134239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114131051..114164562hg38UCSC Ensembl
Innerchr10:115890810..115924321hg19UCSC Ensembl
Innerchr10:115880800..115914311hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3833512
hg1933512
hg1833512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3511533
Samples
Known GenesC10orf118
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045020
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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