A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029340



Internal ID19118559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:134652746..134738436hg38UCSC Ensembl
Innerchr6:134973884..135059574hg19UCSC Ensembl
Innerchr6:135015577..135101267hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3885691
hg1985691
hg1885691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654400
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)nsv1029340
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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