A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046341



Internal ID19135560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126176486..126214411hg38UCSC Ensembl
Innerchr9:128938765..128976690hg19UCSC Ensembl
Innerchr9:127978586..128016511hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3837926
hg1937926
hg1837926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7717n100
Supporting Variantsnssv3695241
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)nsv1046341
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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