A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063834



Internal ID18806365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:2351844..2397786hg38UCSC Ensembl
Innerchr17:2255138..2301080hg19UCSC Ensembl
Innerchr17:2201888..2247830hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3845943
hg1945943
hg1845943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3083n100
Supporting Variantsnssv3560078
Samples
Known GenesMNT, SGSM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063834
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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