A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031214



Internal ID19120435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17382495..17427716hg38UCSC Ensembl
Innerchr5:17382604..17427825hg19UCSC Ensembl
Innerchr5:17435604..17480825hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3845222
hg1945222
hg1845222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5578n100
Supporting Variantsnssv3638310
Samples
Known GenesLOC401177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031214
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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