A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009884



Internal ID19099103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:170001661..170189371hg38UCSC Ensembl
Innerchr3:169719449..169907159hg19UCSC Ensembl
Innerchr3:171202143..171389853hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38187711
hg19187711
hg18187711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3612700
Samples
Known GenesGPR160, PHC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009884
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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