A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048837



Internal ID19138056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105340152..105557234hg38UCSC Ensembl
Innerchr10:107099910..107316992hg19UCSC Ensembl
Innerchr10:107089900..107306982hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38217083
hg19217083
hg18217083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv968n100
Supporting Variantsnssv3706215, nssv3504365
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)nsv1048837
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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