A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052005



Internal ID18794536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133531836..133769367hg38UCSC Ensembl
Innerchr10:135345340..135506692hg19UCSC Ensembl
Innerchr10:135195330..135356682hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38237532
hg19161353
hg18161353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1007n100
Supporting Variantsnssv3503065, nssv3522061
Samples
Known GenesCYP2E1, DUX2, DUX4, DUX4L, DUX4L2, DUX4L3, DUX4L5, DUX4L6, DUX4L7, FRG2B, LOC100653046, SPRNP1, SYCE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052005
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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