A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007404



Internal ID18749935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:621944..1105199hg38UCSC Ensembl
Innerchr3:663627..1146883hg19UCSC Ensembl
Innerchr3:638627..1121883hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38483256
hg19483257
hg18483257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4616n100
Supporting Variantsnssv3590280
Samples
Known GenesCNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007404
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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