A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011838



Internal ID19101056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:175887648..176060147hg38UCSC Ensembl
Innerchr3:175605436..175777935hg19UCSC Ensembl
Innerchr3:177088130..177260629hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38172500
hg19172500
hg18172500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3613626
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011838
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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