A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999860



Internal ID19159396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41529109..41937969hg38UCSC Ensembl
Innerchr3:41570600..41979461hg19UCSC Ensembl
Innerchr3:41545604..41954465hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38408861
hg19408862
hg18408862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4724n100
Supporting Variantsnssv3589710
Samples
Known GenesULK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999860
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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