A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067133



Internal ID19156352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27646266..27754003hg38UCSC Ensembl
Innerchr17:25973292..26081029hg19UCSC Ensembl
Innerchr17:22997419..23105156hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg38107738
hg19107738
hg18107738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3137n100
Supporting Variantsnssv3561042
Samples
Known GenesLGALS9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067133
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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