A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048359



Internal ID19137578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121393547..121435091hg38UCSC Ensembl
Innerchr9:124155825..124197369hg19UCSC Ensembl
Innerchr9:123195646..123237190hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3841545
hg1941545
hg1841545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695219
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)nsv1048359
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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