A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603008



Internal ID16390417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44990635..45114084hg38UCSC Ensembl
Innerchr6:44958372..45081821hg19UCSC Ensembl
Innerchr6:45066350..45189799hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38123450
hg19123450
hg18123450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058426
Samples
Known GenesSUPT3H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603008
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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