A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044482



Internal ID19133701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:25600990..25688341hg38UCSC Ensembl
Innerchr10:25889919..25977270hg19UCSC Ensembl
Innerchr10:25929925..26017276hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3887352
hg1987352
hg1887352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516170
Samples
Known GenesGPR158, LINC00836
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044482
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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