A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615840



Internal ID16403249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134778156..134795468hg38UCSC Ensembl
Innerchr9:137670002..137687314hg19UCSC Ensembl
Innerchr9:136809823..136827135hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3817313
hg1917313
hg1817313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176384
Samples1780862403_A
Known GenesCOL5A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615840
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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