A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028580



Internal ID19117798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119710919..119774392hg38UCSC Ensembl
Innerchr6:120032073..120095538hg19UCSC Ensembl
Innerchr6:120073772..120137237hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3863474
hg1963466
hg1863466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654336
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)nsv1028580
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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