A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049686



Internal ID19138905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42118976..42288034hg38UCSC Ensembl
Innerchr10:42614424..42783482hg19UCSC Ensembl
Innerchr10:41934430..42103488hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38169059
hg19169059
hg18169059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv716n100
Supporting Variantsnssv3512140
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)nsv1049686
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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