A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047432



Internal ID18789963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116633553..116739347hg38UCSC Ensembl
Innerchr9:119395832..119501626hg19UCSC Ensembl
Innerchr9:118435653..118541447hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38105795
hg19105795
hg18105795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695168
Samples
Known GenesASTN2, TRIM32
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047432
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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