A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008881



Internal ID19098099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046103..4056298hg38UCSC Ensembl
Innerchr3:4087787..4097982hg19UCSC Ensembl
Innerchr3:4062787..4072982hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3810196
hg1910196
hg1810196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4645n100
Supporting Variantsnssv3590415, nssv3590416, nssv3739558, nssv3739559
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)nsv1008881
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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