A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061794



Internal ID19151013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27135370..27174126hg38UCSC Ensembl
Innerchr17:25462396..25501152hg19UCSC Ensembl
Innerchr17:22486523..22525279hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3838757
hg1938757
hg1838757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561036
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)nsv1061794
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer