A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1146785



Internal ID15999971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134787857..134809707hg38UCSC Ensembl
Innerchr9:137679703..137701553hg19UCSC Ensembl
Innerchr9:136819524..136841374hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3821851
hg1921851
hg1821851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615841
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)nssv1146785
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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