A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951783



Internal ID16953970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:129584522..129613921hg38UCSC Ensembl
Outerchr9:132346801..132376200hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3829400
hg1929400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996995
SamplesBILGI_BIOE
Known GenesC9orf50, NTMT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951783
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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