A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008844



Internal ID19098062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184469612..184548062hg38UCSC Ensembl
Innerchr3:184187400..184265850hg19UCSC Ensembl
Innerchr3:185670094..185748544hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3878451
hg1978451
hg1878451
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5001n100
Supporting Variantsnssv3615004
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)nsv1008844
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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