A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013334



Internal ID19102552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:239515605..239588394hg38UCSC Ensembl
Innerchr2:240437299..240510088hg19UCSC Ensembl
Innerchr2:240102236..240175025hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3872790
hg1972790
hg1872790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586976
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)nsv1013334
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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