A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998743



Internal ID18811593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8783669..8830534hg38UCSC Ensembl
Innerchr3:8825355..8872219hg19UCSC Ensembl
Innerchr3:8800355..8847219hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3846866
hg1946865
hg1846865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4679n100
Supporting Variantsnssv3739633
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)nsv998743
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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