A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065401



Internal ID19154620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9799828..9986825hg38UCSC Ensembl
Innerchr17:9703145..9890142hg19UCSC Ensembl
Innerchr17:9643870..9830867hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38186998
hg19186998
hg18186998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560341
Samples
Known GenesGAS7, GLP2R, RCVRN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065401
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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