A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040658



Internal ID18783189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:92063743..92100644hg38UCSC Ensembl
Innerchr14:92530087..92566988hg19UCSC Ensembl
Innerchr14:91599840..91636741hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3836902
hg1936902
hg1836902
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1956n100
Supporting Variantsnssv3532590
Samples
Known GenesATXN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040658
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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