A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049877



Internal ID19139096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116836134..116858484hg38UCSC Ensembl
Innerchr9:119598413..119620763hg19UCSC Ensembl
Innerchr9:118638234..118660584hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3822351
hg1922351
hg1822351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695201
Samples
Known GenesASTN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049877
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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