A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060733



Internal ID19149952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:48657855..48698224hg38UCSC Ensembl
Innerchr17:46735217..46775586hg19UCSC Ensembl
Innerchr17:44090216..44130585hg18UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3840370
hg1940370
hg1840370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3262n100
Supporting Variantsnssv3568604
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)nsv1060733
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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