A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061034



Internal ID19150253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13275120..13320898hg38UCSC Ensembl
Innerchr17:13178437..13224215hg19UCSC Ensembl
Innerchr17:13119162..13164940hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3845779
hg1945779
hg1845779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3100n100
Supporting Variantsnssv3560354, nssv3719169
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)nsv1061034
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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