A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041922



Internal ID18784453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94682694..94774471hg38UCSC Ensembl
Innerchr9:97444976..97536753hg19UCSC Ensembl
Innerchr9:96484797..96576574hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3891778
hg1991778
hg1891778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697565
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)nsv1041922
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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