A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003158



Internal ID18745690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66999779..68395539hg38UCSC Ensembl
Innerchr3:67050203..68444689hg19UCSC Ensembl
Innerchr3:67132893..68527379hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381395761
hg191394487
hg181394487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593967
Samples
Known GenesFAM19A1, KBTBD8, MIR4272, SUCLG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003158
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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