A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951788



Internal ID17300662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130655614..130682513hg38UCSC Ensembl
Outerchr9:133531001..133557900hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3826900
hg1926900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997000
SamplesBILGI_BIOE
Known GenesPRDM12
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951788
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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