A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589570



Internal ID16030293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6894157..6918295hg38UCSC Ensembl
Innerchr3:6935844..6959982hg19UCSC Ensembl
Innerchr3:6910844..6934982hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3824139
hg1924139
hg1824139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv958604
Samples
Known GenesGRM7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589570
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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