A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000670



Internal ID18743201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6680357..7004828hg38UCSC Ensembl
Innerchr3:6722044..7046515hg19UCSC Ensembl
Innerchr3:6697044..7021515hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38324472
hg19324472
hg18324472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4674n100
Supporting Variantsnssv3591827
Samples
Known GenesGRM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1000670
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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