A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560297



Internal ID18858578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203166..6235439hg38UCSC Ensembl
Innerchr17:6106486..6138759hg19UCSC Ensembl
Innerchr17:6047210..6079483hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3832274
hg1932274
hg1832274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058437
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)nssv3560297
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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