A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603199



Internal ID16390608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60571733..61107733hg38UCSC Ensembl
Innerchr6:57539480..58075480hg19UCSC Ensembl
Innerchr6:57647439..58183439hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38536001
hg19536001
hg18536001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10678n54
Supporting Variantsnssv1060935
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603199
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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