A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602907



Internal ID16390316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35317943..35344490hg38UCSC Ensembl
Innerchr6:35285720..35312267hg19UCSC Ensembl
Innerchr6:35393698..35420245hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3826548
hg1926548
hg1826548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058197
Samples
Known GenesDEF6, PPARD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602907
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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