A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029550



Internal ID19118769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141051473..141708532hg38UCSC Ensembl
Innerchr6:141372610..142029669hg19UCSC Ensembl
Innerchr6:141414303..142071362hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38657060
hg19657060
hg18657060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654447
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)nsv1029550
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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