A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011096



Internal ID18753630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8452941..8756495hg38UCSC Ensembl
Innerchr3:8494627..8798181hg19UCSC Ensembl
Innerchr3:8469627..8773181hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38303555
hg19303555
hg18303555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591846
Samples
Known GenesCAV3, LINC00312, LMCD1, LMCD1-AS1, OXTR, SSUH2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011096
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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