A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593868



Internal ID18892149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65203548..65231969hg38UCSC Ensembl
Innerchr3:65189223..65217644hg19UCSC Ensembl
Innerchr3:65164263..65192684hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3828422
hg1928422
hg1828422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004636
Supporting Variants
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)nssv3593868
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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