A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040162



Internal ID19129381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132440808..132546416hg38UCSC Ensembl
Innerchr9:135316195..135421803hg19UCSC Ensembl
Innerchr9:134306016..134411624hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38105609
hg19105609
hg18105609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696403
Samples
Known GenesC9orf171
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040162
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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