A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050714



Internal ID19139933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115857024..115927984hg38UCSC Ensembl
Innerchr9:118619303..118690263hg19UCSC Ensembl
Innerchr9:117659124..117730084hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3870961
hg1970961
hg1870961
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695164
Samples
Known GenesLINC00474
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050714
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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