A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604912



Internal ID16392321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:152554727..152605382hg38UCSC Ensembl
Innerchr6:152875862..152926517hg19UCSC Ensembl
Innerchr6:152917555..152968210hg18UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3850656
hg1950656
hg1850656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074596
Samples
Known GenesSYNE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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