A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560226



Internal ID18858507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203166..6229480hg38UCSC Ensembl
Innerchr17:6106486..6132800hg19UCSC Ensembl
Innerchr17:6047210..6073524hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3826315
hg1926315
hg1826315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063963
Supporting Variants
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)nssv3560226
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