A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063354



Internal ID19152573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18722664..18819510hg38UCSC Ensembl
Innerchr17:18625977..18722823hg19UCSC Ensembl
Innerchr17:18566702..18663548hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3896847
hg1996847
hg1896847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719974
Samples
Known GenesFBXW10, TRIM16L, TVP23B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063354
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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