A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv616021



Internal ID16056744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137434689..137452821hg38UCSC Ensembl
Innerchr9:140329141..140347273hg19UCSC Ensembl
Innerchr9:139448962..139467094hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3818133
hg1918133
hg1818133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148376
Samples
Known GenesENTPD8, MIR7114, NSMF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv616021
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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