A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615373



Internal ID16056096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127764326..127817625hg38UCSC Ensembl
Innerchr9:130526605..130579904hg19UCSC Ensembl
Innerchr9:129566426..129619725hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3853300
hg1953300
hg1853300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141631
Samples
Known GenesCDK9, ENG, FPGS, MIR2861, MIR3960, SH2D3C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615373
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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