A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044693



Internal ID19133912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71081369..71119538hg38UCSC Ensembl
Innerchr10:72841126..72879295hg19UCSC Ensembl
Innerchr10:72511132..72549301hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3838170
hg1938170
hg1838170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516361
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)nsv1044693
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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