A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048272



Internal ID19137491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87212064..87435973hg38UCSC Ensembl
Innerchr10:88971821..89195730hg19UCSC Ensembl
Innerchr10:88961801..89185710hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38223910
hg19223910
hg18223910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv949n100
Supporting Variantsnssv3510720
Samples
Known GenesLINC00864, LOC439994, NUTM2A, NUTM2A-AS1, NUTM2D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048272
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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