A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516892



Internal ID18815173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133573736..133769367hg38UCSC Ensembl
Innerchr10:135387240..135506692hg19UCSC Ensembl
Innerchr10:135237230..135356682hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38195632
hg19119453
hg18119453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048457
Supporting Variants
Samples
Known GenesDUX2, DUX4, DUX4L, DUX4L2, DUX4L3, DUX4L5, DUX4L6, DUX4L7, FRG2B, LOC100653046
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3516892
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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