A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052182



Internal ID18794713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:27970213..28072901hg38UCSC Ensembl
Innerchr10:28259142..28361830hg19UCSC Ensembl
Innerchr10:28299148..28401836hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38102689
hg19102689
hg18102689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707745
Samples
Known GenesARMC4, MPP7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052182
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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