A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021707



Internal ID19110925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181018209..181100309hg38UCSC Ensembl
Innerchr5:180445209..180527309hg19UCSC Ensembl
Innerchr5:180377815..180459915hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3882101
hg1982101
hg1882101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5859n100
Supporting Variantsnssv3650339
Samples
Known GenesBTNL9, MIR8089
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021707
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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