A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036316



Internal ID18778847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:702908..804039hg38UCSC Ensembl
Innerchr10:748848..849979hg19UCSC Ensembl
Innerchr10:738848..839979hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38101132
hg19101132
hg18101132
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv654n100
Supporting Variantsnssv3483568
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)nsv1036316
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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