A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008772



Internal ID19097990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99205206..99226554hg38UCSC Ensembl
Innerchr3:98924050..98945398hg19UCSC Ensembl
Innerchr3:100406740..100428088hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3821349
hg1921349
hg1821349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3603388
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)nsv1008772
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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