A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037746



Internal ID18780277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123979237..124002343hg38UCSC Ensembl
Innerchr9:126741516..126764622hg19UCSC Ensembl
Innerchr9:125781337..125804443hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3823107
hg1923107
hg1823107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759825
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)nsv1037746
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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