A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951769



Internal ID16953956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:128101422..128129321hg38UCSC Ensembl
Outerchr9:130863701..130891600hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3827900
hg1927900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996981
SamplesBILGI_BIOE
Known GenesLOC100289019, PTGES2, PTGES2-AS1, SLC25A25
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951769
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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