A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593036



Internal ID16380445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195698774..195714541hg38UCSC Ensembl
Innerchr3:195425645..195441412hg19UCSC Ensembl
Innerchr3:196910825..196927083hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3815768
hg1915768
hg1816259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv986822
Samples
Known GenesMIR570
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593036
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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