A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603094



Internal ID16390503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:51331842..51335305hg38UCSC Ensembl
Innerchr6:51196640..51200103hg19UCSC Ensembl
Innerchr6:51304599..51308062hg18UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg383464
hg193464
hg183464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10657n54
Supporting Variantsnssv1058832, nssv1058834, nssv1058833
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603094
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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