A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1146784



Internal ID15999970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134770065..134795468hg38UCSC Ensembl
Innerchr9:137661911..137687314hg19UCSC Ensembl
Innerchr9:136801732..136827135hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3825404
hg1925404
hg1825404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615839
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)nssv1146784
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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