A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044614



Internal ID18787145
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 StatusM
Merged Variants
Supporting Variantsnssv3759777
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)nsv1044614
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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