A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037412



Internal ID19126631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:107530723..107559956hg38UCSC Ensembl
Innerchr10:109290481..109319714hg19UCSC Ensembl
Innerchr10:109280471..109309704hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3829234
hg1929234
hg1829234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504980
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037412
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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