A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1146782



Internal ID15999968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134767842..134784148hg38UCSC Ensembl
Innerchr9:137659688..137675994hg19UCSC Ensembl
Innerchr9:136799509..136815815hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3816307
hg1916307
hg1816307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615837
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)nssv1146782
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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