A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603036



Internal ID16390445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:48633987..48743404hg38UCSC Ensembl
Innerchr6:48601723..48711041hg19UCSC Ensembl
Innerchr6:48709682..48819000hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38109418
hg19109319
hg18109319
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058570
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603036
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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