A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003314



Internal ID19092533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96561678..96600068hg38UCSC Ensembl
Innerchr3:96280522..96318912hg19UCSC Ensembl
Innerchr3:97763212..97801602hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3838391
hg1938391
hg1838391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4817n100
Supporting Variantsnssv3603307
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)nsv1003314
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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