A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064845



Internal ID19154064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:12259791..12373055hg38UCSC Ensembl
Innerchr17:12163108..12276372hg19UCSC Ensembl
Innerchr17:12103833..12217097hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38113265
hg19113265
hg18113265
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560351
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)nsv1064845
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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