A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045849



Internal ID18788380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94926528..94979054hg38UCSC Ensembl
Innerchr9:97688810..97741336hg19UCSC Ensembl
Innerchr9:96728631..96781157hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3852527
hg1952527
hg1852527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759788
Samples
Known GenesC9orf3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045849
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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