A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036431



Internal ID18778962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116663365..116741547hg38UCSC Ensembl
Innerchr9:119425644..119503826hg19UCSC Ensembl
Innerchr9:118465465..118543647hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3878183
hg1978183
hg1878183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7708n100
Supporting Variantsnssv3759819
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)nsv1036431
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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