A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602934



Internal ID16390343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35790295..35797166hg38UCSC Ensembl
Innerchr6:35758072..35764943hg19UCSC Ensembl
Innerchr6:35866050..35872921hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg386872
hg196872
hg186872
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10630n54
Supporting Variantsnssv1058358, nssv1058359
Samples
Known GenesCLPS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602934
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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