A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058033



Internal ID18800564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:780240..832122hg38UCSC Ensembl
Innerchr17:683480..735362hg19UCSC Ensembl
Innerchr17:630230..682112hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3851883
hg1951883
hg1851883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560052
Samples
Known GenesGLOD4, NXN, RNMTL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058033
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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