A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003199



Internal ID19092417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65203969..65224765hg38UCSC Ensembl
Innerchr3:65189644..65210440hg19UCSC Ensembl
Innerchr3:65164684..65185480hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3820797
hg1920797
hg1820797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4761n100
Supporting Variantsnssv3593900, nssv3593899, nssv3593898, nssv3593897
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)nsv1003199
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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