A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064728



Internal ID18807259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31511259..31545612hg38UCSC Ensembl
Innerchr17:29838277..29872631hg19UCSC Ensembl
Innerchr17:26862397..26896751hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3834354
hg1934355
hg1834355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561051
Samples
Known GenesMIR4724, RAB11FIP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064728
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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