A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604559



Internal ID16045282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:118465323..118792154hg38UCSC Ensembl
Innerchr6:118786486..119113317hg19UCSC Ensembl
Innerchr6:118893179..119220010hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38326832
hg19326832
hg18326832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10918n54
Supporting Variantsnssv1072351
Samples
Known GenesBRD7P3, CEP85L, LOC100287632, PLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604559
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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