A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014521



Internal ID19103739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65203548..65237719hg38UCSC Ensembl
Innerchr3:65189223..65223394hg19UCSC Ensembl
Innerchr3:65164263..65198434hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3834172
hg1934172
hg1834172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4762n100
Supporting Variantsnssv3593872
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)nsv1014521
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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