A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029807



Internal ID19119026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:53443840..53469499hg38UCSC Ensembl
Innerchr6:53308638..53334297hg19UCSC Ensembl
Innerchr6:53416597..53442256hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3825660
hg1925660
hg1825660
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657477
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)nsv1029807
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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