A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007781



Internal ID19097000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3917080..3933034hg38UCSC Ensembl
Innerchr3:3958764..3974718hg19UCSC Ensembl
Innerchr3:3933764..3949718hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3815955
hg1915955
hg1815955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4639n100
Supporting Variantsnssv3590393
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)nsv1007781
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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