A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067269



Internal ID19156488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6392639..6409487hg38UCSC Ensembl
Innerchr17:6295959..6312807hg19UCSC Ensembl
Innerchr17:6236683..6253531hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3816849
hg1916849
hg1816849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3094n100
Supporting Variantsnssv3560321, nssv3560313, nssv3560316, nssv3560320, nssv3560319, nssv3560317, nssv3560314, nssv3560315, nssv3719158, nssv3560318
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)nsv1067269
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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