A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067351



Internal ID19156570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13275120..13347972hg38UCSC Ensembl
Innerchr17:13178437..13251289hg19UCSC Ensembl
Innerchr17:13119162..13192014hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3872853
hg1972853
hg1872853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719174
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)nsv1067351
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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