A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029227



Internal ID19118446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152564834..152620724hg38UCSC Ensembl
Innerchr6:152885969..152941859hg19UCSC Ensembl
Innerchr6:152927662..152983552hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3855891
hg1955891
hg1855891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654476
Samples
Known GenesSYNE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029227
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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