A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615383



Internal ID16056106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128091848..128128781hg38UCSC Ensembl
Innerchr9:130854127..130891060hg19UCSC Ensembl
Innerchr9:129893948..129930881hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3836934
hg1936934
hg1836934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141639
Samples
Known GenesLOC100289019, PTGES2, PTGES2-AS1, SLC25A25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615383
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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