A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053385



Internal ID18795916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129464651..129478805hg38UCSC Ensembl
Innerchr10:131262915..131277069hg19UCSC Ensembl
Innerchr10:131152905..131167059hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3814155
hg1914155
hg1814155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522414
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)nsv1053385
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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