A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv13011n54



Internal ID20146435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137223996..137338927hg38UCSC Ensembl
chr9:140118448..140233379hg19UCSC Ensembl
chr9:139238269..139353200hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38114932
hg19114932
hg18114932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv616019, nsv616018, nsv616020
Samples
Known GenesC9orf169, C9orf173, EXD3, FAM166A, LOC100129722, NELFB, NRARP, RNF224, SLC34A3, TOR4A, TUBB4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv13011n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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