A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009091



Internal ID19098309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:137936746..137972116hg38UCSC Ensembl
Innerchr3:137655588..137690958hg19UCSC Ensembl
Innerchr3:139138278..139173648hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3835371
hg1935371
hg1835371
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3608325
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)nsv1009091
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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