A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043794



Internal ID18786325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129679104..129706404hg38UCSC Ensembl
Innerchr10:131477368..131504668hg19UCSC Ensembl
Innerchr10:131367358..131394658hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3827301
hg1927301
hg1827301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507348
Samples
Known GenesMGMT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043794
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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