A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021307



Internal ID19110524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18095730..18135642hg38UCSC Ensembl
Innerchr8:17953239..17993151hg19UCSC Ensembl
Innerchr8:17997519..18037431hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3839913
hg1939913
hg1839913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7124n100
Supporting Variantsnssv3684188
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021307
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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