A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602958



Internal ID16390367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:38394248..38478858hg38UCSC Ensembl
Innerchr6:38362024..38446634hg19UCSC Ensembl
Innerchr6:38470002..38554612hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3884611
hg1984611
hg1884611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058391
Samples
Known GenesBTBD9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602958
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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