A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047993



Internal ID19137212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82380564..82431969hg38UCSC Ensembl
Innerchr10:84140320..84191725hg19UCSC Ensembl
Innerchr10:84130300..84181705hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3851406
hg1951406
hg1851406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv943n100
Supporting Variantsnssv3706166
Samples
Known GenesNRG3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047993
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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