A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000168



Internal ID18742699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1316180..1330899hg38UCSC Ensembl
Innerchr3:1357864..1372583hg19UCSC Ensembl
Innerchr3:1332864..1347583hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3814720
hg1914720
hg1814720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590309
Samples
Known GenesCNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000168
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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