A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038478



Internal ID19127697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:565930..616748hg38UCSC Ensembl
Innerchr10:611870..662688hg19UCSC Ensembl
Innerchr10:601870..652688hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3850819
hg1950819
hg1850819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv652n100
Supporting Variantsnssv3485733
Samples
Known GenesDIP2C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038478
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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