A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008981



Internal ID19098199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41850072..41947832hg38UCSC Ensembl
Innerchr3:41891564..41989324hg19UCSC Ensembl
Innerchr3:41866568..41964328hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3897761
hg1997761
hg1897761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4725n100
Supporting Variantsnssv3589714
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)nsv1008981
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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