A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1146778



Internal ID15999964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134654313..134655122hg38UCSC Ensembl
Innerchr9:137546159..137546968hg19UCSC Ensembl
Innerchr9:136685980..136686789hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38810
hg19810
hg18810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615834
Supporting Variants
Samples
Known GenesCOL5A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1146778
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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