A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048698



Internal ID19137917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105385380..105548353hg38UCSC Ensembl
Innerchr10:107145138..107308111hg19UCSC Ensembl
Innerchr10:107135128..107298101hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38162974
hg19162974
hg18162974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv968n100
Supporting Variantsnssv3706217
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)nsv1048698
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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