A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038392



Internal ID19127611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:109166226..109283636hg38UCSC Ensembl
Innerchr10:110925984..111043394hg19UCSC Ensembl
Innerchr10:110915974..111033384hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38117411
hg19117411
hg18117411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv973n100
Supporting Variantsnssv3512271, nssv3514953
Samples
Known GenesRNU6-53P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038392
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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