A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006656



Internal ID18749187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:131383932..132145572hg38UCSC Ensembl
Innerchr3:131102776..131864416hg19UCSC Ensembl
Innerchr3:132585466..133347106hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38761641
hg19761641
hg18761641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3607134
Samples
Known GenesCPNE4, MIR5704, MRPL3, NUDT16, SNORA58
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006656
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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