A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043862



Internal ID19133081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121001578..121031196hg38UCSC Ensembl
Innerchr10:122761091..122790709hg19UCSC Ensembl
Innerchr10:122751081..122780699hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3829619
hg1929619
hg1829619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv979n100
Supporting Variantsnssv3507409
Samples
Known GenesMIR5694
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043862
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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