A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759777



Internal ID18711372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77840180..77887820hg38UCSC Ensembl
Innerchr9:80455096..80502736hg19UCSC Ensembl
Innerchr9:79644916..79692556hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3847641
hg1947641
hg1847641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044614
Supporting Variants
Samples
Known GenesGNAQ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3759777
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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